Primary Site >> Stomach Cancer
Gene >> RACGAP1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312377 |
| Start | 50016666:50016666(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765698830 |
| CDS Mutation | c.50G>A |
| AA Mutation | p.Arg17His(p.R17H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312377 |
| Start | 50005289:50005289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.392G>A |
| AA Mutation | p.Gly131Asp(p.G131D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312377 |
| Start | 49990303:49990303(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1864C>A |
| AA Mutation | p.Gln622Lys(p.Q622K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312377 |
| Start | 50005359:50005359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.322A>G |
| AA Mutation | p.Met108Val(p.M108V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312377 |
| Start | 49994229:49994229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1241A>G |
| AA Mutation | p.Asp414Gly(p.D414G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312377 |
| Start | 49994175:49994175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1295C>T |
| AA Mutation | p.Pro432Leu(p.P432L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000312377 |
| Start | 49997125:49997125(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.959G>A |
| AA Mutation | p.Arg320His(p.R320H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312377 |
| Start | 49992305:49992305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1518C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000312377 |
| Start | 50005327:50005327(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149574224 |
| CDS Mutation | c.354C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |