Primary Site >> Pancreatic Cancer
Gene >> RET
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43100555:43100555(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779915615 |
| CDS Mutation | c.170G>A |
| AA Mutation | p.Arg57Gln(p.R57Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43100554:43100554(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.169C>T |
| AA Mutation | p.Arg57Trp(p.R57W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43106495:43106495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.987C>A |
| AA Mutation | p.Phe329Leu(p.F329L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43116714:43116714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2267C>A |
| AA Mutation | p.Ala756Asp(p.A756D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43119668:43119668(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377767424 |
| CDS Mutation | c.2530C>T |
| AA Mutation | p.Arg844Trp(p.R844W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000355710 |
| Start | 43128132:43128132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3208C>T |
| AA Mutation | p.Pro1070Ser(p.P1070S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000355710 |
| Start | 43118396:43118396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775711017 |
| CDS Mutation | c.2308C>T |
| AA Mutation | p.Arg770Ter(p.R770*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |