Primary Site >> Stomach Cancer
Gene >> FBL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221801 |
| Start | 39840482:39840482(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142991383 |
| CDS Mutation | c.215G>A |
| AA Mutation | p.Arg72His(p.R72H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221801 |
| Start | 39837720:39837720(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.673A>G |
| AA Mutation | p.Met225Val(p.M225V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221801 |
| Start | 39837723:39837723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.670C>A |
| AA Mutation | p.Arg224Ser(p.R224S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221801 |
| Start | 39837801:39837801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377432606 |
| CDS Mutation | c.592C>T |
| AA Mutation | p.Arg198Cys(p.R198C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000221801 |
| Start | 39837727:39837727(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.666A>C |
| AA Mutation | p.Lys222Asn(p.K222N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221801 |
| Start | 39840633:39840633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746722061 |
| CDS Mutation | c.165A>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000221801 |
| Start | 39840427:39840427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369326013 |
| CDS Mutation | c.270G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |