Primary Site >> Stomach Cancer
Gene >> GCFC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321027 |
| Start | 75690049:75690049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1259G>A |
| AA Mutation | p.Gly420Glu(p.G420E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321027 |
| Start | 75694386:75694386(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.875A>G |
| AA Mutation | p.Glu292Gly(p.E292G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321027 |
| Start | 75670175:75670175(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2066C>T |
| AA Mutation | p.Ala689Val(p.A689V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321027 |
| Start | 75694423:75694423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.838A>G |
| AA Mutation | p.Thr280Ala(p.T280A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321027 |
| Start | 75702369:75702369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.449C>T |
| AA Mutation | p.Ala150Val(p.A150V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321027 |
| Start | 75710821:75710821(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.35G>A |
| AA Mutation | p.Arg12His(p.R12H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000321027 |
| Start | 75702370:75702370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.448G>A |
| AA Mutation | p.Ala150Thr(p.A150T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000321027 |
| Start | 75694373:75694373(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147763714 |
| CDS Mutation | c.888C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321027 |
| Start | 75670148:75670148(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2093delA |
| AA Mutation | p.Lys698SerfsTer5(p.K698Sfs*5) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000321027 |
| Start | 75689171:75689172(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1393dupT |
| AA Mutation | p.Cys465LeufsTer2(p.C465Lfs*2) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |