Primary Site >> Stomach Cancer
Gene >> RBMS3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383767 |
| Start | 29739742:29739742(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.422A>G |
| AA Mutation | p.Asn141Ser(p.N141S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383767 |
| Start | 29739725:29739725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.405A>T |
| AA Mutation | p.Gln135His(p.Q135H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383767 |
| Start | 29897438:29897438(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.851C>T |
| AA Mutation | p.Thr284Met(p.T284M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383767 |
| Start | 29488494:29488494(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.302G>A |
| AA Mutation | p.Cys101Tyr(p.C101Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383767 |
| Start | 29587149:29587149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.343G>A |
| AA Mutation | p.Ala115Thr(p.A115T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383767 |
| Start | 29587159:29587159(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.353C>T |
| AA Mutation | p.Ala118Val(p.A118V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383767 |
| Start | 29988192:29988192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199569162 |
| CDS Mutation | c.1148C>T |
| AA Mutation | p.Thr383Met(p.T383M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000383767 |
| Start | 29897413:29897413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376210051 |
| CDS Mutation | c.826C>T |
| AA Mutation | p.Arg276Cys(p.R276C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000383767 |
| Start | 29884191:29884191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.774A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000383767 |
| Start | 29884196:29884196(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.780delC |
| AA Mutation | p.Ile261TyrfsTer17(p.I261Yfs*17) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000383767 |
| Start | 29868908:29868908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763252410 |
| CDS Mutation | c.688C>T |
| AA Mutation | p.Arg230Ter(p.R230*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |