Primary Site >> Stomach Cancer
Gene >> CRTC1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321949 |
| Start | 18760087:18760087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.745C>A |
| AA Mutation | p.Leu249Met(p.L249M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321949 |
| Start | 18765457:18765457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774556926 |
| CDS Mutation | c.940C>G |
| AA Mutation | p.Leu314Val(p.L314V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321949 |
| Start | 18771508:18771508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1387G>A |
| AA Mutation | p.Val463Ile(p.V463I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321949 |
| Start | 18765419:18765419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.902G>A |
| AA Mutation | p.Gly301Asp(p.G301D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321949 |
| Start | 18745887:18745887(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.308G>T |
| AA Mutation | p.Arg103Met(p.R103M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321949 |
| Start | 18777244:18777244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764408980 |
| CDS Mutation | c.1767C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321949 |
| Start | 18765432:18765432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781723836 |
| CDS Mutation | c.915G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321949 |
| Start | 18775769:18775769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777830005 |
| CDS Mutation | c.1641G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321949 |
| Start | 18775670:18775670(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1542C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321949 |
| Start | 18768744:18768744(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1277delC |
| AA Mutation | p.Pro426GlnfsTer85(p.P426Qfs*85) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321949 |
| Start | 18777183:18777183(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs779900748 |
| CDS Mutation | c.1713delC |
| AA Mutation | p.Ser572AlafsTer6(p.S572Afs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |