Primary Site >> Stomach Cancer
Gene >> GLS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311966 |
| Start | 56474877:56474877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1016A>G |
| AA Mutation | p.Asp339Gly(p.D339G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311966 |
| Start | 56474591:56474591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1177A>G |
| AA Mutation | p.Met393Val(p.M393V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311966 |
| Start | 56473265:56473265(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771248266 |
| CDS Mutation | c.1412G>A |
| AA Mutation | p.Arg471Gln(p.R471Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311966 |
| Start | 56474579:56474579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752169894 |
| CDS Mutation | c.1189G>A |
| AA Mutation | p.Gly397Ser(p.G397S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311966 |
| Start | 56473532:56473532(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1287G>A |
| AA Mutation | p.Met429Ile(p.M429I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311966 |
| Start | 56474592:56474592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1176C>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311966 |
| Start | 56479172:56479172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.414C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311966 |
| Start | 56480384:56480384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.186T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000311966 |
| Start | 56472694:56472694(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754953103 |
| CDS Mutation | c.1507C>T |
| AA Mutation | p.Arg503Ter(p.R503*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |