19-10230138-C-CAGTGGCATGGGAGGA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230138
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230153
    reference: chr 19
allele count: 1
allele frequency: 7.717240314863405e-5
allele num: 12958
alternate allele: CAGTGGCATGGGAGGA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24818
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

19-10230155-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230155
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230155
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 12426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.301C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+175C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+175C>G
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29734
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD

19-10230157-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230157
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230157
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 11924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.299C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+173C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+173C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30081
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

19-10230168-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230168
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230168
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 11276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.288C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+162C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+162C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33711
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

19-10230173-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230173
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230173
    reference: chr 19
allele count: 1
allele frequency: 8.865248226950355e-5
allele num: 11280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.283G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+157G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+157G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35084
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/19-10230174-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230174
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230174
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 11290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.282T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+156T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+156T>G
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35433
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

19-10230175-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230175
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230175
    reference: chr 19
allele count: 1
allele frequency: 9.023641941887746e-5
allele num: 11082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.281G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+155G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35644
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

19-10230176-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230176
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230176
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 10952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.280G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+154G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+154G>C
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35878
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-10230198-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230198
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230198
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 9898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.258G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+132G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+132G>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

19-10230213-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230213
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230213
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 9446
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.243C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+117C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+117C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15946
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

19-10230217-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230217
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230217
    reference: chr 19
allele count: 1
allele frequency: 1.042318115488847e-4
allele num: 9594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.239C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+113C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+113C>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18062
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

19-10230222-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230222
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230222
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 10452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.234C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+108C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+108C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

19-10230235-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230235
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230235
    reference: chr 19
allele count: 1
allele frequency: 7.840677434530344e-5
allele num: 12754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.221G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+95G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+95G>C
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20881
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-10230236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230236
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230236
    reference: chr 19
allele count: 2
allele frequency: 1.495215311004785e-4
allele num: 13376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.220C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+94C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+94C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19636
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/19-10230243-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230243
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230243
    reference: chr 19
allele count: 3
allele frequency: 1.639344262295082e-4
allele num: 18300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.213T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+87T>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+87T>G
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13885
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

19-10230245-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230245
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230245
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 20360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.211C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+85C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+85C>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37295
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

19-10230250-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230250
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230250
    reference: chr 19
allele count: 8
allele frequency: 3.137254901960784e-4
allele num: 25500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.206G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+80G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+80G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9397
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5466
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37685
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

19-10230251-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230251
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230251
    reference: chr 19
allele count: 1
allele frequency: 3.727726832177738e-5
allele num: 26826
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.205T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+79T>C
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8782
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

19-10230255-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230255
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230255
    reference: chr 19
allele count: 3
allele frequency: 9.328358208955224e-5
allele num: 32160
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.201A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+75A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+75A>C
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36873
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

19-10230267-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230267
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230267
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 47244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.189C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+63C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+63C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31057
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

19-10230271-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230271
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230271
    reference: chr 19
allele count: 1
allele frequency: 1.844201829448215e-5
allele num: 54224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.185C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+59C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+59C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-10230276-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230276
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230276
    reference: chr 19
allele count: 5
allele frequency: 7.972447222399387e-5
allele num: 62716
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.180T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+54T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+54T>C
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4421
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/19-10230279-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230279
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230279
    reference: chr 19
allele count: 1
allele frequency: 1.513225591671206e-5
allele num: 66084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.177G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+51G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+51G>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23155
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

19-10230291-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230291
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230291
    reference: chr 19
allele count: 3
allele frequency: 3.819904247733523e-5
allele num: 78536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.165C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+39C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27776
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS

http://identifiers.org/exac.variant/19-10230293-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230293
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230293
    reference: chr 19
allele count: 59
allele frequency: 7.289710388455076e-4
allele num: 80936
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.163G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+37G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+37G>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

19-10230297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230297
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230297
    reference: chr 19
allele count: 1
allele frequency: 1.19115685153421e-5
allele num: 83952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.159G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+33G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-10230298-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230298
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230298
    reference: chr 19
allele count: 1
allele frequency: 1.17057639181533e-5
allele num: 85428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.158G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+32G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+32G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3772
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13463
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

19-10230301-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230301
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230301
    reference: chr 19
allele count: 2
allele frequency: 2.270147559591373e-5
allele num: 88100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.155C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+29C>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+29C>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30809
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/19-10230306-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230306
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230306
    reference: chr 19
allele count: 1
allele frequency: 1.100763930167536e-5
allele num: 90846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.150G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+24G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+24G>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/19-10230307-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230307
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230307
    reference: chr 19
allele count: 1
allele frequency: 1.090869422930075e-5
allele num: 91670
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.149G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+23G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+23G>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-10230318-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230318
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230318
    reference: chr 19
allele count: 1
allele frequency: 1.015909137086779e-5
allele num: 98434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.67+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.138C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.67+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.67+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.195+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.47+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.128+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.67+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.83+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.67+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.67+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.116+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.67+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.67+12C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.113+12C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7815
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

19-10230338-CCCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230338
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230335
    reference: chr 19
allele count: 2
allele frequency: 1.894441708028644e-5
allele num: 105572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.56_58delAGG
  hgvsp: ENSP00000465882.1:p.Glu19del
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.184_186delAGG
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.105_107delAGG
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.56_58delAGG
  hgvsp: ENSP00000253108.3:p.Glu19del
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.56_58delAGG
  hgvsp: ENSP00000468159.1:p.Glu19del
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.56_58delAGG
  hgvsp: ENSP00000466943.1:p.Glu19del
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.115_117delAGG
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.56_58delAGG
  hgvsp: ENSP00000468313.1:p.Glu19del
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.117_119delAGG
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.72_74delAGG
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.56_58delAGG
  hgvsp: ENSP00000466860.1:p.Glu19del
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.36_38delAGG
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.56_58delAGG
  hgvsp: ENSP00000465925.1:p.Glu19del
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.56_58delAGG
  hgvsp: ENSP00000465933.1:p.Glu19del
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.102_104delAGG
  variant of: http://identifiers.org/hgnc/3274
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu19del
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: CCCT
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

19-10230340-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230340
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230340
    reference: chr 19
allele count: 1
allele frequency: 9.41105610871652e-6
allele num: 106258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.57G>C
  hgvsp: ENSP00000465933.1:p.Glu19Asp
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.103G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.116G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.57G>C
  hgvsp: ENSP00000253108.3:p.Glu19Asp
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.57G>C
  hgvsp: ENSP00000468159.1:p.Glu19Asp
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.106G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.37G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.57G>C
  hgvsp: ENSP00000465882.1:p.Glu19Asp
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.185G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.73G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.57G>C
  hgvsp: ENSP00000468313.1:p.Glu19Asp
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.57G>C
  hgvsp: ENSP00000466860.1:p.Glu19Asp
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.57G>C
  hgvsp: ENSP00000465925.1:p.Glu19Asp
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.57G>C
  hgvsp: ENSP00000466943.1:p.Glu19Asp
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.118G>C
  variant of: http://identifiers.org/hgnc/3274
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35722
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu19Asp
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

19-10230340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230340
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230340
    reference: chr 19
allele count: 3
allele frequency: 2.823316832614956e-5
allele num: 106258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.57G>A
  hgvsp: ENST00000588709.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.37G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.57G>A
  hgvsp: ENST00000587993.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.118G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.116G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.57G>A
  hgvsp: ENST00000589454.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.57G>A
  hgvsp: ENST00000587146.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.73G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.57G>A
  hgvsp: ENST00000593095.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.57G>A
  hgvsp: ENST00000593066.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.106G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.185G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.57G>A
  hgvsp: ENST00000253108.4:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.57G>A
  hgvsp: ENST00000586151.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.103G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35722
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu19Glu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

19-10230364-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230364
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230364
    reference: chr 19
allele count: 1
allele frequency: 8.948545861297538e-6
allele num: 111750
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.79T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.33T>C
  hgvsp: ENST00000587146.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.92T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.94T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.33T>C
  hgvsp: ENST00000588709.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.49T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.33T>C
  hgvsp: ENST00000593066.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.33T>C
  hgvsp: ENST00000253108.4:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.82T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.33T>C
  hgvsp: ENST00000587993.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.33T>C
  hgvsp: ENST00000593095.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.161T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.33T>C
  hgvsp: ENST00000586151.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.33T>C
  hgvsp: ENST00000589454.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser11Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

19-10230370-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230370
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230370
    reference: chr 19
allele count: 1
allele frequency: 8.867606632969762e-6
allele num: 112770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.27G>A
  hgvsp: ENST00000588709.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.27G>A
  hgvsp: ENST00000589454.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.27G>A
  hgvsp: ENST00000253108.4:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.86G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.155G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.27G>A
  hgvsp: ENST00000593095.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.27G>A
  hgvsp: ENST00000586151.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.27G>A
  hgvsp: ENST00000593066.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.27G>A
  hgvsp: ENST00000587146.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.76G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.7G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.88G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.43G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.73G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.27G>A
  hgvsp: ENST00000587993.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3274
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4789
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Lys9Lys
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff

19-10230374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230374
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230374
    reference: chr 19
allele count: 1
allele frequency: 8.779631255487269e-6
allele num: 113900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.23C>T
  hgvsp: ENSP00000465882.1:p.Ser8Leu
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.23C>T
  hgvsp: ENSP00000253108.3:p.Ser8Leu
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.23C>T
  hgvsp: ENSP00000468313.1:p.Ser8Leu
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.23C>T
  hgvsp: ENSP00000466860.1:p.Ser8Leu
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.23C>T
  hgvsp: ENSP00000468159.1:p.Ser8Leu
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.23C>T
  hgvsp: ENSP00000466943.1:p.Ser8Leu
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.69C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.23C>T
  hgvsp: ENSP00000465925.1:p.Ser8Leu
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.82C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000590940
  gene symbol: EIF3G
  hgvsc: ENST00000590940.1:n.3C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.72C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.84C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.23C>T
  hgvsp: ENSP00000465933.1:p.Ser8Leu
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.151C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12626
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser8Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

19-10230377-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230377
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230377
    reference: chr 19
allele count: 1
allele frequency: 8.721437292865864e-6
allele num: 114660
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.148G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-1G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-1G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: true
consequence: splice acceptor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12786
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.21-1G>A
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/19-10230380-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230380
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230380
    reference: chr 19
allele count: 1
allele frequency: 8.663559336717898e-6
allele num: 115426
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.145G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-4G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-4G>T
  variant of: http://identifiers.org/hgnc/3274
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.21-4G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-10230380-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230380
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230380
    reference: chr 19
allele count: 6
allele frequency: 5.198135602030738e-5
allele num: 115426
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.145G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-4G>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-4G>C
  variant of: http://identifiers.org/hgnc/3274
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12960
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.21-4G>C
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP

19-10230380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230380
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230380
    reference: chr 19
allele count: 83
allele frequency: 7.190754249475855e-4
allele num: 115426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-4G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.145G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-4G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36974
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: c.21-4G>A
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

19-10230389-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230389
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230389
    reference: chr 19
allele count: 1
allele frequency: 8.512232077495362e-6
allele num: 117478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.136T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-13T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-13T>C
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-10230392-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230392
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230392
    reference: chr 19
allele count: 2
allele frequency: 1.695576241585703e-5
allele num: 117954
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.133A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-16A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-16A>G
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

19-10230392-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230392
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230392
    reference: chr 19
allele count: 1
allele frequency: 8.477881207928515e-6
allele num: 117954
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.133A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-16A>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-16A>C
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

19-10230398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230398
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230398
    reference: chr 19
allele count: 1
allele frequency: 8.423890152472412e-6
allele num: 118710
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.127C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-22C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-22C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13705
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

19-10230407-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230407
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230407
    reference: chr 19
allele count: 1
allele frequency: 8.344598541364175e-6
allele num: 119838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.118A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-31A>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-31A>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

19-10230414-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230414
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230414
    reference: chr 19
allele count: 13
allele frequency: 1.080290515049278e-4
allele num: 120338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.111T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-38T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-38T>C
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6092
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14250
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

19-10230415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230415
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230415
    reference: chr 19
allele count: 2
allele frequency: 1.661515967168445e-5
allele num: 120372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.110C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-39C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-39C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

19-10230416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230416
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230416
    reference: chr 19
allele count: 3
allele frequency: 2.491652962575373e-5
allele num: 120402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.109G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-40G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-40G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6201
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-10230422-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230422
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230422
    reference: chr 19
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.103G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-46G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-46G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-10230423-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230423
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230423
    reference: chr 19
allele count: 1
allele frequency: 8.279105194310599e-6
allele num: 120786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-47G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.102G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-47G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-10230428-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230428
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230428
    reference: chr 19
allele count: 1
allele frequency: 8.270888127967181e-6
allele num: 120906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.82-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.21-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.21-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.37-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.97G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.21-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.21-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.21-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.21-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.70-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.21-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.67-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.80-52G>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.21-52G>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14515
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-10230466-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230466
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230466
    reference: chr 19
allele count: 5
allele frequency: 4.122147473948028e-5
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.59G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+50G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+50G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

19-10230468-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230468
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230468
    reference: chr 19
allele count: 3
allele frequency: 2.473329266080762e-5
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.57C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+48C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+48C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

19-10230468-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230468
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230468
    reference: chr 19
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.57C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+48C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+48C>G
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

19-10230469-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230469
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230469
    reference: chr 19
allele count: 7
allele frequency: 5.770911309337334e-5
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.56T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+47T>C
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+47T>C
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8093
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11596
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

19-10230470-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230470
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230470
    reference: chr 19
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.55C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+46C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+46C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

19-10230470-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230470
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230470
    reference: chr 19
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.55C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+46C>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+46C>G
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5937
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9765
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/19-10230476-C-CAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230476
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230478
    reference: chr 19
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: CAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+38_66+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+38_20+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+38_20+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+38_20+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+38_20+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+38_20+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+38_36+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+38_20+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+38_20+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+38_79+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.47_48dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+38_81+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+38_69+39dupTT
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+38_20+39dupTT
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

19-10230484-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230484
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230484
    reference: chr 19
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.41A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+32A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+32A>G
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9757
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

19-10230490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230490
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230490
    reference: chr 19
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.35C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+26C>T
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+26C>T
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

19-10230491-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230491
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230491
    reference: chr 19
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+25G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.34G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9760
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-10230492-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230492
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230492
    reference: chr 19
allele count: 4
allele frequency: 3.299785513941594e-5
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.33G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+24G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+24G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4409
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

19-10230497-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230497
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230497
    reference: chr 19
allele count: 9
allele frequency: 7.425252458583592e-5
allele num: 121208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.28A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+19A>G
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+19A>G
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-10230498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10230498
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 10230498
    reference: chr 19
allele count: 2
allele frequency: 1.650137786505173e-5
allele num: 121202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466860
  ensembl transcript: ENST00000589454
  gene symbol: EIF3G
  hgvsc: ENST00000589454.1:c.20+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000466943
  ensembl transcript: ENST00000593066
  gene symbol: EIF3G
  hgvsc: ENST00000593066.1:c.20+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465882
  ensembl transcript: ENST00000588709
  gene symbol: EIF3G
  hgvsc: ENST00000588709.1:c.20+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587590
  gene symbol: EIF3G
  hgvsc: ENST00000587590.1:n.36+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589458
  gene symbol: EIF3G
  hgvsc: ENST00000589458.1:n.81+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587681
  gene symbol: EIF3G
  hgvsc: ENST00000587681.1:n.69+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468159
  ensembl transcript: ENST00000587146
  gene symbol: EIF3G
  hgvsc: ENST00000587146.1:c.20+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465933
  ensembl transcript: ENST00000593095
  gene symbol: EIF3G
  hgvsc: ENST00000593095.1:c.20+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000253108
  ensembl transcript: ENST00000253108
  gene symbol: EIF3G
  hgvsc: ENST00000253108.4:c.20+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000468313
  ensembl transcript: ENST00000587993
  gene symbol: EIF3G
  hgvsc: ENST00000587993.1:c.20+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000587168
  gene symbol: EIF3G
  hgvsc: ENST00000587168.1:n.27G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000589009
  gene symbol: EIF3G
  hgvsc: ENST00000589009.1:n.66+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl transcript: ENST00000592485
  gene symbol: EIF3G
  hgvsc: ENST00000592485.1:n.79+18G>A
  variant of: http://identifiers.org/hgnc/3274
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000130811
  ensembl protein: ENSP00000465925
  ensembl transcript: ENST00000586151
  gene symbol: EIF3G
  hgvsc: ENST00000586151.1:c.20+18G>A
  variant of: http://identifiers.org/hgnc/3274
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7365
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: C

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

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

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

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

GenotypeDepth
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2152
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22634
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2283
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 715
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 44
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.335826876836762e-4
allele num: 7486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3980
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.15e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

MQ
type: SiteQuality
SIO_000300: 5.606e1

DP
type: SiteQuality
SIO_000300: 2.28441e5

QD
type: SiteQuality
SIO_000300: 2.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.851e0

VQSLOD
type: SiteQuality
SIO_000300: -1.533e0

MQRankSum
type: SiteQuality
SIO_000300: -2.883e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.238e0

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

GenotypeDepth
all individuals: 363
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2097
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3647
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 126
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3610
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27036
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 2684
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3755
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.68e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.28506e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.3e-2

QD
type: SiteQuality
SIO_000300: 1.847e1

GenotypeDepth
all individuals: 1731
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3985
bin: 7.5e0
variant carriers: 0

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

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

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

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

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

GenotypeDepth
all individuals: 12
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 378
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3306
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2900
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26763
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 4161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.39e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.18977e5

VQSLOD
type: SiteQuality
SIO_000300: 3.11e0

QD
type: SiteQuality
SIO_000300: 1.48e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 5433
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 2095
bin: 1.25e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 1716
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2292
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 553
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30740
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 75
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5749
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5814
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 944
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3824
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 1.484e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.22e-1

DP
type: SiteQuality
SIO_000300: 2.20193e5

VQSLOD
type: SiteQuality
SIO_000300: -3.432e-1

MQ
type: SiteQuality
SIO_000300: 4.822e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.38e-2

GenotypeDepth
all individuals: 539
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2286
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6158
bin: 7.5e0
variant carriers: 0

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

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

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

GenotypeDepth
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African
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MQ
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DP
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FS
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Latino
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European (Non-Finnish)
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African
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South Asian
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MQ
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FS
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DP
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European (Finnish)
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African
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Latino
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East Asian
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MQ
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QD
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DP
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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European (Finnish)
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East Asian
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African
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VQSLOD
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DP
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ReadPosRankSum
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FS
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MQ
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MQ
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VQSLOD
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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allele num: 4844
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East Asian
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European (Finnish)
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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MQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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African
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QD
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MQ
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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South Asian
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East Asian
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allele frequency: 0.0e0
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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QD
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DP
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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Other
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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MQ
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Other
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European (Non-Finnish)
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African
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Latino
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VQSLOD
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QD
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FS
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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MQ
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DP
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 8
allele frequency: 2.28310502283105e-3
allele num: 3504
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

VQSLOD
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DP
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ReadPosRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -1.9e-2

BaseQRankSum
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FS
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MQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 3600
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 6.2266500622665e-5
allele num: 16060
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1764
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1944
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2136
num of homozygotes: 0

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

MQ
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SIO_000300: 6.0e1

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3980
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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2198
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 1.549106681813488e-4
allele num: 19366
num of homozygotes: 1

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: -1.37e-2

ClippingRankSum
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SIO_000300: 9.22e-1

MQRankSum
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SIO_000300: 0.0e0

VQSLOD
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ReadPosRankSum
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FS
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BaseQRankSum
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QD
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SIO_000300: 1.208e1

MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 5.92868e5

GenotypeDepth
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variant carriers: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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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 num: 32930
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 1.452643811737362e-4
allele num: 6884
num of homozygotes: 0

Other
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FS
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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MQ
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 6.397679774801672e-5
allele num: 46892
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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QD
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BaseQRankSum
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MQ
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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DP
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 5.676657584014533e-4
allele num: 8808
num of homozygotes: 0

African
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allele frequency: 4.107338444687842e-4
allele num: 7304
num of homozygotes: 0

European (Non-Finnish)
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allele count: 50
allele frequency: 1.036484245439469e-3
allele num: 48240
num of homozygotes: 0

European (Finnish)
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allele frequency: 2.487562189054726e-4
allele num: 4020
num of homozygotes: 0

East Asian
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South Asian
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Other
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MQRankSum
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SIO_000300: 6.7e-2

VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.004008016032064e-5
allele num: 49900
num of homozygotes: 0

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

Latino
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European (Finnish)
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Other
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South Asian
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allele frequency: 1.471453796350795e-4
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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MQ
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MQRankSum
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VQSLOD
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 7036
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Latino
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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South Asian
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DP
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BaseQRankSum
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InbreedingCoeff
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QD
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MQ
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Other
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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FS
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 61114
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64068
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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South Asian
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allele num: 12306
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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DP
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MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

East Asian
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Other
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European (Non-Finnish)
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African
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Latino
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South Asian
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FS
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ReadPosRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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BaseQRankSum
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VQSLOD
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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Latino
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African
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European (Finnish)
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East Asian
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MQ
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BaseQRankSum
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VQSLOD
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MQRankSum
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QD
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DP
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FS
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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MQ
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BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele count: 2
allele frequency: 3.048780487804878e-4
allele num: 6560
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 2.624212736179146e-4
allele num: 11432
num of homozygotes: 0

European (Non-Finnish)
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allele count: 74
allele frequency: 1.147429138497798e-3
allele num: 64492
num of homozygotes: 0

African
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allele frequency: 3.914660403210022e-4
allele num: 10218
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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FS
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65106
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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allele num: 14556
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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DP
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

South Asian
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allele frequency: 0.0e0
allele num: 14852
num of homozygotes: 0

Latino
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allele frequency: 1.741856819369448e-4
allele num: 11482
num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11482
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.53261402648357e-5
allele num: 65248
num of homozygotes: 0

InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.526251526251526e-5
allele num: 65520
num of homozygotes: 0

South Asian
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African
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Other
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European (Finnish)
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Latino
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East Asian
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DP
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QD
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MQ
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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African
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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VQSLOD
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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MQRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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allele num: 66104
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Latino
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South Asian
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Other
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East Asian
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DP
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InbreedingCoeff
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VQSLOD
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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MQRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

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

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

European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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Latino
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South Asian
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African
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DP
type: SiteQuality
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MQ
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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QD
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FS
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SIO_000300: 1.232e0

MQRankSum
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SIO_000300: 2.03e0

VQSLOD
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ClippingRankSum
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SIO_000300: -1.514e0

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

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

Other
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South Asian
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European (Finnish)
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Latino
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African
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European (Non-Finnish)
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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FS
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SIO_000300: 4.517e0

MQRankSum
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SIO_000300: 1.03e0

BaseQRankSum
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MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.711865e6

QD
type: SiteQuality
SIO_000300: 1.255e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

East Asian
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African
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Latino
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European (Non-Finnish)
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Other
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South Asian
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DP
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.880000000000001e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 2

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

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

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