Primary Site >> Stomach Cancer
Gene >> HGD
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283871 |
| Start | 120633238:120633238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1097G>T |
| AA Mutation | p.Ser366Ile(p.S366I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283871 |
| Start | 120646315:120646315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.601T>G |
| AA Mutation | p.Leu201Val(p.L201V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283871 |
| Start | 120670479:120670479(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.230A>G |
| AA Mutation | p.Asp77Gly(p.D77G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000283871 |
| Start | 120641677:120641677(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.791A>G |
| AA Mutation | p.Asn264Ser(p.N264S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000283871 |
| Start | 120650806:120650806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.402C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000283871 |
| Start | 120633223:120633224(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs397515516 |
| CDS Mutation | c.1111dupC |
| AA Mutation | p.His371ProfsTer4(p.H371Pfs*4) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |