Primary Site >> Stomach Cancer
Gene >> MYCT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367245 |
| Start | 152698065:152698065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.163A>G |
| AA Mutation | p.Ser55Gly(p.S55G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367245 |
| Start | 152721933:152721933(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.388G>A |
| AA Mutation | p.Gly130Ser(p.G130S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367245 |
| Start | 152697970:152697970(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.68G>A |
| AA Mutation | p.Arg23Lys(p.R23K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367245 |
| Start | 152721925:152721925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201917444 |
| CDS Mutation | c.380G>A |
| AA Mutation | p.Arg127His(p.R127H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367245 |
| Start | 152722156:152722156(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375330501 |
| CDS Mutation | c.611G>A |
| AA Mutation | p.Arg204His(p.R204H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367245 |
| Start | 152698065:152698065(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.163A>C |
| AA Mutation | p.Ser55Arg(p.S55R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367245 |
| Start | 152721840:152721840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.295G>T |
| AA Mutation | p.Ala99Ser(p.A99S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367245 |
| Start | 152698057:152698057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.155A>C |
| AA Mutation | p.Asn52Thr(p.N52T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367245 |
| Start | 152721926:152721926(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768361552 |
| CDS Mutation | c.381C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |