Primary Site >> Stomach Cancer
Gene >> LGR4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379214 |
| Start | 27372360:27372360(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1418T>A |
| AA Mutation | p.Phe473Tyr(p.F473Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379214 |
| Start | 27369008:27369008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761830490 |
| CDS Mutation | c.1715C>T |
| AA Mutation | p.Ser572Leu(p.S572L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379214 |
| Start | 27368475:27368475(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149204548 |
| CDS Mutation | c.2248G>A |
| AA Mutation | p.Ala750Thr(p.A750T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379214 |
| Start | 27373633:27373633(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1297C>A |
| AA Mutation | p.Leu433Met(p.L433M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379214 |
| Start | 27382243:27382243(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.703A>G |
| AA Mutation | p.Asn235Asp(p.N235D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379214 |
| Start | 27384366:27384366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.659G>A |
| AA Mutation | p.Cys220Tyr(p.C220Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379214 |
| Start | 27368621:27368621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369897268 |
| CDS Mutation | c.2102C>T |
| AA Mutation | p.Thr701Met(p.T701M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000379214 |
| Start | 27412791:27412791(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.255G>C |
| AA Mutation | p.Glu85Asp(p.E85D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379214 |
| Start | 27372291:27372291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1487A>C |
| AA Mutation | p.Gln496Pro(p.Q496P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000379214 |
| Start | 27368431:27368431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs138381781 |
| CDS Mutation | c.2292G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |