Primary Site >> Stomach Cancer
Gene >> KLF12
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377669 |
| Start | 73813200:73813200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.758T>G |
| AA Mutation | p.Val253Gly(p.V253G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377669 |
| Start | 73846144:73846144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150943448 |
| CDS Mutation | c.353C>T |
| AA Mutation | p.Ser118Leu(p.S118L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377669 |
| Start | 73846255:73846255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.242C>T |
| AA Mutation | p.Pro81Leu(p.P81L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000377669 |
| Start | 73715454:73715454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.941G>A |
| AA Mutation | p.Arg314Gln(p.R314Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377669 |
| Start | 73813181:73813181(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371400583 |
| CDS Mutation | c.777G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377669 |
| Start | 73846299:73846299(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750790792 |
| CDS Mutation | c.198G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000377669 |
| Start | 73845858:73845858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs571821638 |
| CDS Mutation | c.639G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000377669 |
| Start | 73695672:73695672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1028-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |