Primary Site >> Stomach Cancer
Gene >> PKM
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335181 |
| Start | 72219004:72219004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776788433 |
| CDS Mutation | c.94C>T |
| AA Mutation | p.Arg32Cys(p.R32C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335181 |
| Start | 72209726:72209726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.512G>A |
| AA Mutation | p.Gly171Asp(p.G171D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335181 |
| Start | 72209807:72209807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771478196 |
| CDS Mutation | c.431T>C |
| AA Mutation | p.Leu144Pro(p.L144P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335181 |
| Start | 72200564:72200564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746373368 |
| CDS Mutation | c.1399C>T |
| AA Mutation | p.Arg467Cys(p.R467C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335181 |
| Start | 72208871:72208871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.586G>A |
| AA Mutation | p.Glu196Lys(p.E196K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335181 |
| Start | 72202521:72202521(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1240G>A |
| AA Mutation | p.Val414Met(p.V414M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335181 |
| Start | 72206852:72206852(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs2959910 |
| CDS Mutation | c.1016G>A |
| AA Mutation | p.Arg339His(p.R339H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335181 |
| Start | 72218952:72218952(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.146G>A |
| AA Mutation | p.Cys49Tyr(p.C49Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335181 |
| Start | 72202481:72202481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1280C>T |
| AA Mutation | p.Ala427Val(p.A427V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335181 |
| Start | 72210450:72210450(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.275G>A |
| AA Mutation | p.Arg92His(p.R92H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335181 |
| Start | 72207262:72207262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.852G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335181 |
| Start | 72208791:72208791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11558356 |
| CDS Mutation | c.666G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335181 |
| Start | 72206743:72206743(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1125G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335181 |
| Start | 72219092:72219092(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764776324 |
| CDS Mutation | c.6G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335181 |
| Start | 72219053:72219053(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.45C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335181 |
| Start | 72207157:72207157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.957A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |