Primary Site >> Stomach Cancer
Gene >> KLF15
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296233 |
| Start | 126351946:126351946(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.977C>A |
| AA Mutation | p.Pro326His(p.P326H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296233 |
| Start | 126352588:126352588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139892976 |
| CDS Mutation | c.335C>T |
| AA Mutation | p.Ala112Val(p.A112V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296233 |
| Start | 126352504:126352504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.419C>T |
| AA Mutation | p.Thr140Ile(p.T140I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296233 |
| Start | 126352261:126352261(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.662T>C |
| AA Mutation | p.Leu221Pro(p.L221P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296233 |
| Start | 126343744:126343744(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752858408 |
| CDS Mutation | c.1234G>A |
| AA Mutation | p.Val412Met(p.V412M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296233 |
| Start | 126352394:126352394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.529C>T |
| AA Mutation | p.Pro177Ser(p.P177S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296233 |
| Start | 126343749:126343749(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1229G>A |
| AA Mutation | p.Arg410His(p.R410H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000296233 |
| Start | 126351869:126351869(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376424318 |
| CDS Mutation | c.1054G>A |
| AA Mutation | p.Ala352Thr(p.A352T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |