Primary Site >> Stomach Cancer
Gene >> CD40LG
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370629 |
| Start | 136656392:136656392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.383G>C |
| AA Mutation | p.Ser128Thr(p.S128T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370629 |
| Start | 136659127:136659127(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.498A>C |
| AA Mutation | p.Gln166His(p.Q166H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000370629 |
| Start | 136650396:136650396(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.287A>G |
| AA Mutation | p.Lys96Arg(p.K96R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370629 |
| Start | 136659212:136659212(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.583C>G |
| AA Mutation | p.Leu195Val(p.L195V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370629 |
| Start | 136654399:136654399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778398894 |
| CDS Mutation | c.315G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370629 |
| Start | 136656399:136656399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.390C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370629 |
| Start | 136659283:136659283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368157256 |
| CDS Mutation | c.654C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370629 |
| Start | 136656378:136656378(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148581967 |
| CDS Mutation | c.369G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |