Primary Site >> Stomach Cancer
Gene >> FSCN1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382361 |
| Start | 5603283:5603283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.859G>A |
| AA Mutation | p.Glu287Lys(p.E287K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382361 |
| Start | 5593040:5593040(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.104C>T |
| AA Mutation | p.Ala35Val(p.A35V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382361 |
| Start | 5593289:5593289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.353G>A |
| AA Mutation | p.Arg118His(p.R118H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382361 |
| Start | 5593664:5593664(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.728G>A |
| AA Mutation | p.Gly243Asp(p.G243D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382361 |
| Start | 5593138:5593138(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.202C>T |
| AA Mutation | p.Arg68Cys(p.R68C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382361 |
| Start | 5593420:5593420(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.484G>A |
| AA Mutation | p.Glu162Lys(p.E162K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382361 |
| Start | 5603552:5603552(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754279900 |
| CDS Mutation | c.1046C>T |
| AA Mutation | p.Ala349Val(p.A349V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000382361 |
| Start | 5603528:5603528(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377275041 |
| CDS Mutation | c.1022G>A |
| AA Mutation | p.Arg341His(p.R341H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382361 |
| Start | 5593161:5593161(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.225C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382361 |
| Start | 5593506:5593506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.570C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382361 |
| Start | 5603918:5603918(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776771373 |
| CDS Mutation | c.1167C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000382361 |
| Start | 5605312:5605312(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs564738398 |
| CDS Mutation | c.1320G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |