Primary Site >> Stomach Cancer
Gene >> GML
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220940 |
| Start | 142840441:142840441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4C>A |
| AA Mutation | p.Leu2Ile(p.L2I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220940 |
| Start | 142840502:142840502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200642476 |
| CDS Mutation | c.65G>A |
| AA Mutation | p.Arg22His(p.R22H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220940 |
| Start | 142846635:142846635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.422T>C |
| AA Mutation | p.Val141Ala(p.V141A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220940 |
| Start | 142846658:142846658(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.445G>T |
| AA Mutation | p.Ala149Ser(p.A149S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220940 |
| Start | 142846572:142846572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.359G>T |
| AA Mutation | p.Arg120Met(p.R120M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220940 |
| Start | 142846456:142846456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.243T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220940 |
| Start | 142840503:142840503(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138131984 |
| CDS Mutation | c.66C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |