Primary Site >> Stomach Cancer
Gene >> CTSH
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220166 |
| Start | 78927745:78927745(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377571418 |
| CDS Mutation | c.667G>A |
| AA Mutation | p.Gly223Ser(p.G223S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220166 |
| Start | 78937404:78937404(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769006889 |
| CDS Mutation | c.143C>T |
| AA Mutation | p.Thr48Met(p.T48M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220166 |
| Start | 78923060:78923060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.865G>A |
| AA Mutation | p.Gly289Arg(p.G289R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220166 |
| Start | 78923044:78923044(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.881T>C |
| AA Mutation | p.Ile294Thr(p.I294T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000220166 |
| Start | 78937348:78937348(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201782561 |
| CDS Mutation | c.199G>A |
| AA Mutation | p.Ala67Thr(p.A67T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220166 |
| Start | 78937412:78937412(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.135C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000220166 |
| Start | 78932450:78932450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776428294 |
| CDS Mutation | c.414C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000220166 |
| Start | 78923050:78923050(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.875delA |
| AA Mutation | p.Asn292MetfsTer8(p.N292Mfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |