Primary Site >> Stomach Cancer
Gene >> LILRB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54632590:54632590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374212814 |
| CDS Mutation | c.788G>A |
| AA Mutation | p.Arg263His(p.R263H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54632102:54632102(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.526G>A |
| AA Mutation | p.Gly176Arg(p.G176R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54632608:54632608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.806C>G |
| AA Mutation | p.Ala269Gly(p.A269G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54635275:54635275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779583013 |
| CDS Mutation | c.1579G>A |
| AA Mutation | p.Asp527Asn(p.D527N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54636498:54636498(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1658G>T |
| AA Mutation | p.Ser553Ile(p.S553I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54633049:54633049(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.992A>T |
| AA Mutation | p.Gln331Leu(p.Q331L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54631620:54631620(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.191A>C |
| AA Mutation | p.Lys64Thr(p.K64T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54635116:54635116(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1499C>A |
| AA Mutation | p.Ala500Asp(p.A500D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54632730:54632730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.928C>A |
| AA Mutation | p.Pro310Thr(p.P310T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54631599:54631599(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.170A>G |
| AA Mutation | p.Glu57Gly(p.E57G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54632069:54632069(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.493C>A |
| AA Mutation | p.Pro165Thr(p.P165T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000324602 |
| Start | 54632613:54632613(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201049465 |
| CDS Mutation | c.811G>A |
| AA Mutation | p.Ala271Thr(p.A271T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |