Primary Site >> Stomach Cancer
Gene >> NOTUM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409678 |
| Start | 81956913:81956913(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.857C>T |
| AA Mutation | p.Ala286Val(p.A286V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409678 |
| Start | 81953022:81953022(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1430T>C |
| AA Mutation | p.Val477Ala(p.V477A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000409678 |
| Start | 81953174:81953174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1278G>T |
| AA Mutation | p.Lys426Asn(p.K426N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409678 |
| Start | 81960706:81960706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.204G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409678 |
| Start | 81955513:81955513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs568603969 |
| CDS Mutation | c.1020C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000409678 |
| Start | 81953114:81953114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763866532 |
| CDS Mutation | c.1338C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000409678 |
| Start | 81957066:81957066(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.704delG |
| AA Mutation | p.Gly235AlafsTer6(p.G235Afs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000409678 |
| Start | 81953153:81953153(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1299delC |
| AA Mutation | p.Val434SerfsTer28(p.V434Sfs*28) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000409678 |
| Start | 81960723:81960724(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.186_187delCA |
| AA Mutation | p.Met63GlyfsTer123(p.M63Gfs*123) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000409678 |
| Start | 81953095:81953095(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746437719 |
| CDS Mutation | c.1357C>T |
| AA Mutation | p.Arg453Ter(p.R453*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |