Primary Site >> Stomach Cancer
Gene >> KIR3DL1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391728 |
| Start | 54819897:54819897(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.540C>A |
| AA Mutation | p.Phe180Leu(p.F180L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391728 |
| Start | 54818492:54818492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.248G>T |
| AA Mutation | p.Ser83Ile(p.S83I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391728 |
| Start | 54830174:54830174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1234A>T |
| AA Mutation | p.Thr412Ser(p.T412S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391728 |
| Start | 54818398:54818398(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777577843 |
| CDS Mutation | c.154C>T |
| AA Mutation | p.Arg52Cys(p.R52C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391728 |
| Start | 54819828:54819828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.471A>C |
| AA Mutation | p.Lys157Asn(p.K157N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000391728 |
| Start | 54818596:54818596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.352A>C |
| AA Mutation | p.Thr118Pro(p.T118P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391728 |
| Start | 54818499:54818499(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.255G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000391728 |
| Start | 54829950:54829950(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1128G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000391728 |
| Start | 54818365:54818365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376509720 |
| CDS Mutation | c.121C>T |
| AA Mutation | p.Arg41Ter(p.R41*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000391728 |
| Start | 54821771:54821771(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.862G>T |
| AA Mutation | p.Gly288Ter(p.G288*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |