Primary Site >> Stomach Cancer
Gene >> FOSL2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264716 |
| Start | 28408787:28408787(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.383G>A |
| AA Mutation | p.Arg128His(p.R128H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264716 |
| Start | 28412063:28412063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.596G>C |
| AA Mutation | p.Arg199Pro(p.R199P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264716 |
| Start | 28404233:28404233(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.229C>A |
| AA Mutation | p.Pro77Thr(p.P77T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264716 |
| Start | 28408859:28408859(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.455T>G |
| AA Mutation | p.Leu152Arg(p.L152R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264716 |
| Start | 28412236:28412236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763475600 |
| CDS Mutation | c.769G>A |
| AA Mutation | p.Gly257Ser(p.G257S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264716 |
| Start | 28404237:28404237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375020008 |
| CDS Mutation | c.233G>A |
| AA Mutation | p.Arg78His(p.R78H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264716 |
| Start | 28408840:28408840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.436C>T |
| AA Mutation | p.Arg146Trp(p.R146W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264716 |
| Start | 28412396:28412396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.929G>T |
| AA Mutation | p.Ser310Ile(p.S310I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264716 |
| Start | 28404212:28404212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.208A>G |
| AA Mutation | p.Thr70Ala(p.T70A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264716 |
| Start | 28408829:28408829(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.425G>A |
| AA Mutation | p.Arg142Gln(p.R142Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264716 |
| Start | 28404160:28404160(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs112541505 |
| CDS Mutation | c.156C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264716 |
| Start | 28408842:28408842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.438G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264716 |
| Start | 28412397:28412397(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141121352 |
| CDS Mutation | c.930C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000264716 |
| Start | 28404355:28404356(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.352dupC |
| AA Mutation | p.Gln118ProfsTer5(p.Q118Pfs*5) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |