Primary Site >> Stomach Cancer
Gene >> RNF38
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259605 |
| Start | 36369777:36369777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.512T>C |
| AA Mutation | p.Leu171Pro(p.L171P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259605 |
| Start | 36369783:36369783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.506G>A |
| AA Mutation | p.Arg169His(p.R169H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259605 |
| Start | 36369873:36369873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.416G>C |
| AA Mutation | p.Ser139Thr(p.S139T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259605 |
| Start | 36339766:36339766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1534C>T |
| AA Mutation | p.Arg512Trp(p.R512W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000259605 |
| Start | 36357897:36357897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs183475137 |
| CDS Mutation | c.616G>A |
| AA Mutation | p.Ala206Thr(p.A206T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000259605 |
| Start | 36357925:36357925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.588C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000259605 |
| Start | 36390593:36390593(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149578872 |
| CDS Mutation | c.36A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000259605 |
| Start | 36353243:36353243(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.998delC |
| AA Mutation | p.Pro333GlnfsTer12(p.P333Qfs*12) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000259605 |
| Start | 36351130:36351130(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1248delA |
| AA Mutation | p.Val417Ter(p.V417*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |