Primary Site >> Stomach Cancer
Gene >> CTNNBL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361383 |
| Start | 37859948:37859948(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1442T>A |
| AA Mutation | p.Phe481Tyr(p.F481Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361383 |
| Start | 37779302:37779302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998G>A |
| AA Mutation | p.Gly333Asp(p.G333D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361383 |
| Start | 37746529:37746529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767022909 |
| CDS Mutation | c.388A>G |
| AA Mutation | p.Met130Val(p.M130V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361383 |
| Start | 37871975:37871975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1654G>A |
| AA Mutation | p.Glu552Lys(p.E552K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361383 |
| Start | 37871992:37871992(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1671G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361383 |
| Start | 37859937:37859937(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774471300 |
| CDS Mutation | c.1431C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000361383 |
| Start | 37777706:37777706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.876G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000361383 |
| Start | 37733014:37733014(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs761516328 |
| CDS Mutation | c.172delA |
| AA Mutation | p.Arg58GlyfsTer25(p.R58Gfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000361383 |
| Start | 37860305:37860305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760040999 |
| CDS Mutation | c.1564C>T |
| AA Mutation | p.Arg522Ter(p.R522*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000361383 |
| Start | 37802973:37802973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751223032 |
| CDS Mutation | c.1138C>T |
| AA Mutation | p.Arg380Ter(p.R380*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |