Primary Site >> Stomach Cancer
Gene >> NEFL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955642:24955642(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.874G>A |
| AA Mutation | p.Ala292Thr(p.A292T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24953695:24953695(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570772656 |
| CDS Mutation | c.1270T>C |
| AA Mutation | p.Tyr424His(p.Y424H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955798:24955798(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.718T>C |
| AA Mutation | p.Tyr240His(p.Y240H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955587:24955587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.929G>A |
| AA Mutation | p.Arg310His(p.R310H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24956218:24956218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.298C>T |
| AA Mutation | p.Arg100Cys(p.R100C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955624:24955624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.892G>A |
| AA Mutation | p.Val298Met(p.V298M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24956283:24956283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.233C>A |
| AA Mutation | p.Ala78Asp(p.A78D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955558:24955558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.958G>A |
| AA Mutation | p.Glu320Lys(p.E320K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24954218:24954218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1132G>A |
| AA Mutation | p.Val378Met(p.V378M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955879:24955879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.637A>G |
| AA Mutation | p.Ile213Val(p.I213V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955549:24955549(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764562926 |
| CDS Mutation | c.967C>T |
| AA Mutation | p.Arg323Trp(p.R323W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955989:24955989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.527C>T |
| AA Mutation | p.Ala176Val(p.A176V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955756:24955756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.760C>T |
| AA Mutation | p.Leu254Phe(p.L254F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610854 |
| Start | 24953690:24953690(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs114329068 |
| CDS Mutation | c.1275C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610854 |
| Start | 24956105:24956105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.411G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955691:24955691(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.825C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955796:24955796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs58975336 |
| CDS Mutation | c.720C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955838:24955838(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.678G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610854 |
| Start | 24955745:24955745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.771G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610854 |
| Start | 24953780:24953780(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751512030 |
| CDS Mutation | c.1185C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000610854 |
| Start | 24956369:24956369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.147C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000610854 |
| Start | 24953552:24953552(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1413delC |
| AA Mutation | p.Ser472LeufsTer78(p.S472Lfs*78) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |