Primary Site >> Stomach Cancer
Gene >> RCC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375433 |
| Start | 17409151:17409151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1508A>C |
| AA Mutation | p.Glu503Ala(p.E503A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000375433 |
| Start | 17420828:17420828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.745A>C |
| AA Mutation | p.Ile249Leu(p.I249L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375433 |
| Start | 17422756:17422756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.604G>A |
| AA Mutation | p.Glu202Lys(p.E202K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375433 |
| Start | 17422827:17422827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.533A>G |
| AA Mutation | p.Glu178Gly(p.E178G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375433 |
| Start | 17412147:17412147(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1361G>A |
| AA Mutation | p.Gly454Asp(p.G454D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375433 |
| Start | 17420730:17420730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.843T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000375433 |
| Start | 17416621:17416621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs188700442 |
| CDS Mutation | c.885C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000375433 |
| Start | 17409101:17409101(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1558delC |
| AA Mutation | p.Arg520GlufsTer55(p.R520Efs*55) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000375433 |
| Start | 17413116:17413118(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1268_1270delCAG |
| AA Mutation | p.Ala423del(p.A423del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | start_lost |
| Transcription ID | ENST00000375433 |
| Start | 17438513:17438513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2T>C |
| AA Mutation | p.Met1?(p.M1?) |
| Mutation Classification | Translation_Start_Site |
| Feature Type | Transcript |