Primary Site >> Stomach Cancer
Gene >> CORIN
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47786817:47786817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140958503 |
| CDS Mutation | c.317G>A |
| AA Mutation | p.Ser106Asn(p.S106N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47623671:47623671(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2440C>T |
| AA Mutation | p.Pro814Ser(p.P814S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47603484:47603484(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs182487045 |
| CDS Mutation | c.2725C>T |
| AA Mutation | p.Arg909Trp(p.R909W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47744564:47744564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.637A>G |
| AA Mutation | p.Arg213Gly(p.R213G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47680161:47680161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370951437 |
| CDS Mutation | c.1112A>C |
| AA Mutation | p.Lys371Thr(p.K371T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47665198:47665198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1423A>C |
| AA Mutation | p.Asn475His(p.N475H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47763383:47763383(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759707115 |
| CDS Mutation | c.613G>T |
| AA Mutation | p.Asp205Tyr(p.D205Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47661828:47661828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1618T>C |
| AA Mutation | p.Cys540Arg(p.C540R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47603647:47603647(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2562G>C |
| AA Mutation | p.Trp854Cys(p.W854C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47623733:47623733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143333327 |
| CDS Mutation | c.2378G>A |
| AA Mutation | p.Arg793His(p.R793H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47744522:47744522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.679C>A |
| AA Mutation | p.Leu227Met(p.L227M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000273857 |
| Start | 47661831:47661831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201223301 |
| CDS Mutation | c.1615C>T |
| AA Mutation | p.Arg539Cys(p.R539C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273857 |
| Start | 47595877:47595877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754465485 |
| CDS Mutation | c.2973T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273857 |
| Start | 47786834:47786834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.300T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273857 |
| Start | 47595769:47595769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376673462 |
| CDS Mutation | c.3081C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273857 |
| Start | 47600244:47600244(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2916C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273857 |
| Start | 47744496:47744496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs755107174 |
| CDS Mutation | c.705G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000273857 |
| Start | 47643207:47643207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2007A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000273857 |
| Start | 47661834:47661834(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1612G>T |
| AA Mutation | p.Glu538Ter(p.E538*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000273857 |
| Start | 47645178:47645179(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs773653221 |
| CDS Mutation | c.1858_1859dupGA |
| AA Mutation | p.Asp620GlufsTer13(p.D620Efs*13) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |