Primary Site >> Stomach Cancer
Gene >> RNF216
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5741623:5741623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371431845 |
| CDS Mutation | c.223G>A |
| AA Mutation | p.Gly75Ser(p.G75S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5715124:5715124(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141012211 |
| CDS Mutation | c.1591G>A |
| AA Mutation | p.Ala531Thr(p.A531T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5741474:5741474(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.372G>T |
| AA Mutation | p.Leu124Phe(p.L124F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5641324:5641324(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2041G>A |
| AA Mutation | p.Gly681Ser(p.G681S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5741396:5741396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.450G>T |
| AA Mutation | p.Glu150Asp(p.E150D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000425013 |
| Start | 5740974:5740974(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs557865990 |
| CDS Mutation | c.872C>T |
| AA Mutation | p.Thr291Met(p.T291M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5752881:5752881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166G>A |
| AA Mutation | p.Glu56Lys(p.E56K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5623108:5623108(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2353C>A |
| AA Mutation | p.Pro785Thr(p.P785T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5622867:5622867(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778491862 |
| CDS Mutation | c.2594G>A |
| AA Mutation | p.Arg865His(p.R865H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5711819:5711819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377674225 |
| CDS Mutation | c.1832C>T |
| AA Mutation | p.Pro611Leu(p.P611L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5652429:5652429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1972A>G |
| AA Mutation | p.Lys658Glu(p.K658E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425013 |
| Start | 5741289:5741289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747054051 |
| CDS Mutation | c.557G>A |
| AA Mutation | p.Arg186His(p.R186H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425013 |
| Start | 5622932:5622932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777676348 |
| CDS Mutation | c.2529C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425013 |
| Start | 5623055:5623055(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200420546 |
| CDS Mutation | c.2406C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425013 |
| Start | 5712756:5712756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200434435 |
| CDS Mutation | c.1770C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425013 |
| Start | 5729495:5729495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1155C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425013 |
| Start | 5712741:5712741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141187642 |
| CDS Mutation | c.1785G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425013 |
| Start | 5752957:5752957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.90G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000425013 |
| Start | 5725415:5725415(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1242delA |
| AA Mutation | p.Lys414AsnfsTer19(p.K414Nfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000425013 |
| Start | 5741031:5741031(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.815G>A |
| AA Mutation | p.Trp272Ter(p.W272*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | stop_lost |
| Transcription ID | ENST00000425013 |
| Start | 5622860:5622860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748840697 |
| CDS Mutation | c.2601A>G |
| AA Mutation | p.Ter867TrpextTer15(p.*867Wext*15) |
| Mutation Classification | Nonstop_Mutation |
| Feature Type | Transcript |