Primary Site >> Stomach Cancer
Gene >> RNF26
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311413 |
| Start | 119336359:119336359(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777702624 |
| CDS Mutation | c.1237G>A |
| AA Mutation | p.Val413Ile(p.V413I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311413 |
| Start | 119336378:119336378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779473222 |
| CDS Mutation | c.1256C>T |
| AA Mutation | p.Pro419Leu(p.P419L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311413 |
| Start | 119336403:119336403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1281G>T |
| AA Mutation | p.Gln427His(p.Q427H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311413 |
| Start | 119335249:119335249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773328736 |
| CDS Mutation | c.127G>A |
| AA Mutation | p.Val43Ile(p.V43I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311413 |
| Start | 119335330:119335330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.208G>A |
| AA Mutation | p.Glu70Lys(p.E70K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311413 |
| Start | 119336167:119336167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150700766 |
| CDS Mutation | c.1045C>T |
| AA Mutation | p.Pro349Ser(p.P349S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311413 |
| Start | 119335957:119335957(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150176910 |
| CDS Mutation | c.835C>T |
| AA Mutation | p.Arg279Cys(p.R279C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311413 |
| Start | 119336030:119336030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs144743618 |
| CDS Mutation | c.908G>A |
| AA Mutation | p.Arg303Gln(p.R303Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |