Primary Site >> Stomach Cancer
Gene >> GCK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403799 |
| Start | 44149778:44149778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs193922317 |
| CDS Mutation | c.661G>A |
| AA Mutation | p.Glu221Lys(p.E221K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403799 |
| Start | 44153403:44153403(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762263694 |
| CDS Mutation | c.106C>T |
| AA Mutation | p.Arg36Trp(p.R36W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403799 |
| Start | 44149977:44149977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.571C>T |
| AA Mutation | p.Arg191Trp(p.R191W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403799 |
| Start | 44152384:44152384(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.250T>G |
| AA Mutation | p.Phe84Val(p.F84V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403799 |
| Start | 44145621:44145621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1129C>T |
| AA Mutation | p.Arg377Cys(p.R377C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403799 |
| Start | 44146508:44146508(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.974G>A |
| AA Mutation | p.Arg325His(p.R325H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403799 |
| Start | 44147762:44147762(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.751A>C |
| AA Mutation | p.Met251Leu(p.M251L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000403799 |
| Start | 44147738:44147738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.775G>A |
| AA Mutation | p.Ala259Thr(p.A259T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000403799 |
| Start | 44146519:44146519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753628968 |
| CDS Mutation | c.963C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000403799 |
| Start | 44151070:44151070(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.369C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000403799 |
| Start | 44153451:44153451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.58C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000403799 |
| Start | 44149779:44149779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142952813 |
| CDS Mutation | c.660C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |