Primary Site >> Stomach Cancer
Gene >> GCG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375497 |
| Start | 162147413:162147413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.194A>G |
| AA Mutation | p.Tyr65Cys(p.Y65C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375497 |
| Start | 162145661:162145661(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.271C>T |
| AA Mutation | p.Arg91Cys(p.R91C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375497 |
| Start | 162144126:162144126(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.437A>G |
| AA Mutation | p.His146Arg(p.H146R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375497 |
| Start | 162144087:162144087(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.476T>C |
| AA Mutation | p.Leu159Pro(p.L159P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375497 |
| Start | 162147377:162147377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.230G>T |
| AA Mutation | p.Trp77Leu(p.W77L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000375497 |
| Start | 162145660:162145660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs35920035 |
| CDS Mutation | c.272G>A |
| AA Mutation | p.Arg91His(p.R91H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |