| 401867195 | CV2472821 | single nucleotide variant | NM_001568.3(EIF3E):c.25C>T (p.Arg9Cys) | not provided [RCV003331518] | uncertain significance | 8 | 108248678 | 108248678 | Human | | name |
| 405719978 | CV3238591 | single nucleotide variant | NM_001568.3(EIF3E):c.35A>C (p.His12Pro) | not specified [RCV004377786] | uncertain significance | 8 | 108248668 | 108248668 | Human | | name |
| 405719151 | CV3238592 | single nucleotide variant | NM_001568.3(EIF3E):c.56T>G (p.Val19Gly) | not specified [RCV004377787] | uncertain significance | 8 | 108248647 | 108248647 | Human | | name |
| 597664306 | CV3674463 | single nucleotide variant | NM_001568.3(EIF3E):c.944G>A (p.Cys315Tyr) | not specified [RCV004912308] | uncertain significance | 8 | 108216419 | 108216419 | Human | | name |
| 597665200 | CV3674464 | single nucleotide variant | NM_001568.3(EIF3E):c.332G>A (p.Arg111Lys) | not specified [RCV004912309] | uncertain significance | 8 | 108236195 | 108236195 | Human | | name |
| 597746622 | CV3674465 | single nucleotide variant | NM_001568.3(EIF3E):c.835A>G (p.Lys279Glu) | not specified [RCV004922731] | uncertain significance | 8 | 108217348 | 108217348 | Human | | name |
| 598179225 | CV3961371 | single nucleotide variant | NM_001568.3(EIF3E):c.578A>G (p.Lys193Arg) | not specified [RCV005332473] | uncertain significance | 8 | 108229089 | 108229089 | Human | | name |
| 598179231 | CV3961372 | single nucleotide variant | NM_001568.3(EIF3E):c.660T>G (p.Phe220Leu) | not specified [RCV005332474] | uncertain significance | 8 | 108228329 | 108228329 | Human | | name |
| 155923674 | CV2212337 | single nucleotide variant | NM_001568.3(EIF3E):c.1072G>C (p.Asp358His) | not specified [RCV004091284] | uncertain significance | 8 | 108203493 | 108203493 | Human | | name |