Primary Site >> Stomach Cancer
Gene >> RAP1GAP
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374765 |
| Start | 21602873:21602873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1469C>T |
| AA Mutation | p.Ser490Leu(p.S490L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374765 |
| Start | 21611774:21611774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771544929 |
| CDS Mutation | c.655G>A |
| AA Mutation | p.Ala219Thr(p.A219T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374765 |
| Start | 21598448:21598448(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1831A>G |
| AA Mutation | p.Thr611Ala(p.T611A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374765 |
| Start | 21598445:21598445(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1834T>C |
| AA Mutation | p.Trp612Arg(p.W612R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374765 |
| Start | 21601735:21601735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763968945 |
| CDS Mutation | c.1601C>T |
| AA Mutation | p.Ser534Leu(p.S534L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000374765 |
| Start | 21620015:21620015(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.18G>T |
| AA Mutation | p.Gln6His(p.Q6H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374765 |
| Start | 21608307:21608307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1202T>C |
| AA Mutation | p.Leu401Pro(p.L401P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374765 |
| Start | 21599511:21599511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1759G>A |
| AA Mutation | p.Gly587Arg(p.G587R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374765 |
| Start | 21602844:21602844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376776052 |
| CDS Mutation | c.1498G>A |
| AA Mutation | p.Ala500Thr(p.A500T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374765 |
| Start | 21602889:21602889(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1453C>T |
| AA Mutation | p.Pro485Ser(p.P485S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000374765 |
| Start | 21611568:21611568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.727C>A |
| AA Mutation | p.Leu243Met(p.L243M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374765 |
| Start | 21599614:21599614(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1656G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000374765 |
| Start | 21611461:21611461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201554924 |
| CDS Mutation | c.834C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |