Primary Site >> Stomach Cancer
Gene >> KLHL23
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272797 |
| Start | 169735429:169735429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.415T>C |
| AA Mutation | p.Cys139Arg(p.C139R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272797 |
| Start | 169749707:169749707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1652G>A |
| AA Mutation | p.Gly551Glu(p.G551E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272797 |
| Start | 169736003:169736003(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751896737 |
| CDS Mutation | c.989C>T |
| AA Mutation | p.Thr330Met(p.T330M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272797 |
| Start | 169736175:169736175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1161G>C |
| AA Mutation | p.Glu387Asp(p.E387D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272797 |
| Start | 169735120:169735120(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.106A>T |
| AA Mutation | p.Thr36Ser(p.T36S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000272797 |
| Start | 169741504:169741504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1333G>A |
| AA Mutation | p.Glu445Lys(p.E445K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000272797 |
| Start | 169749558:169749558(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781533649 |
| CDS Mutation | c.1503C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |