Primary Site >> Stomach Cancer
Gene >> MARK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220653349:220653349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373048949 |
| CDS Mutation | c.1985G>A |
| AA Mutation | p.Arg662His(p.R662H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220650692:220650692(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs780288227 |
| CDS Mutation | c.1543G>A |
| AA Mutation | p.Val515Ile(p.V515I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220618371:220618371(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.614A>G |
| AA Mutation | p.Asn205Ser(p.N205S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220662089:220662089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2311C>T |
| AA Mutation | p.Arg771Cys(p.R771C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220652144:220652144(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1730G>A |
| AA Mutation | p.Arg577Gln(p.R577Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000366917 |
| Start | 220579370:220579370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.68G>T |
| AA Mutation | p.Gly23Val(p.G23V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366917 |
| Start | 220618432:220618432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775657431 |
| CDS Mutation | c.675C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000366917 |
| Start | 220662016:220662016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141632214 |
| CDS Mutation | c.2238C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |