Primary Site >> Stomach Cancer
Gene >> WNT10A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258411 |
| Start | 218882210:218882210(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.163C>T |
| AA Mutation | p.Leu55Phe(p.L55F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258411 |
| Start | 218890037:218890037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs570082664 |
| CDS Mutation | c.430G>A |
| AA Mutation | p.Ala144Thr(p.A144T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258411 |
| Start | 218890040:218890040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs543063101 |
| CDS Mutation | c.433G>A |
| AA Mutation | p.Val145Met(p.V145M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258411 |
| Start | 218892862:218892862(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.845A>T |
| AA Mutation | p.Glu282Val(p.E282V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000258411 |
| Start | 218882207:218882207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375821607 |
| CDS Mutation | c.160G>A |
| AA Mutation | p.Val54Met(p.V54M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258411 |
| Start | 218881086:218881086(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.91C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258411 |
| Start | 218882206:218882206(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143421847 |
| CDS Mutation | c.159C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258411 |
| Start | 218892797:218892797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.780G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000258411 |
| Start | 218893178:218893178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1161G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000258411 |
| Start | 218882194:218882194(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs749297006 |
| CDS Mutation | c.152delC |
| AA Mutation | p.Pro51ArgfsTer12(p.P51Rfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |