Primary Site >> Stomach Cancer
Gene >> AFAP1L2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304129 |
| Start | 114323240:114323240(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.337G>C |
| AA Mutation | p.Ala113Pro(p.A113P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304129 |
| Start | 114297338:114297338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374605165 |
| CDS Mutation | c.2189G>A |
| AA Mutation | p.Arg730His(p.R730H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304129 |
| Start | 114296061:114296061(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2438A>T |
| AA Mutation | p.Glu813Val(p.E813V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304129 |
| Start | 114297398:114297398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752318393 |
| CDS Mutation | c.2129C>T |
| AA Mutation | p.Ala710Val(p.A710V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304129 |
| Start | 114315622:114315622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748304962 |
| CDS Mutation | c.550C>T |
| AA Mutation | p.Arg184Cys(p.R184C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304129 |
| Start | 114304923:114304923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1080G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304129 |
| Start | 114300315:114300315(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770242787 |
| CDS Mutation | c.1836C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304129 |
| Start | 114313925:114313925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs11196688 |
| CDS Mutation | c.738C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000304129 |
| Start | 114300630:114300630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1603C>T |
| AA Mutation | p.Arg535Ter(p.R535*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |