Primary Site >> Stomach Cancer
Gene >> ANGPTL6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253109 |
| Start | 10093745:10093745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.899A>T |
| AA Mutation | p.Gln300Leu(p.Q300L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253109 |
| Start | 10094806:10094806(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.715G>T |
| AA Mutation | p.Ala239Ser(p.A239S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253109 |
| Start | 10092698:10092698(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1304G>A |
| AA Mutation | p.Gly435Asp(p.G435D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253109 |
| Start | 10093739:10093739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.905G>T |
| AA Mutation | p.Arg302Met(p.R302M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253109 |
| Start | 10093568:10093568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1003T>C |
| AA Mutation | p.Tyr335His(p.Y335H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000253109 |
| Start | 10092618:10092618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780477052 |
| CDS Mutation | c.1384G>A |
| AA Mutation | p.Ala462Thr(p.A462T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000253109 |
| Start | 10092700:10092700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138536720 |
| CDS Mutation | c.1302C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |