Primary Site >> Stomach Cancer
Gene >> S1PR4
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246115 |
| Start | 3179237:3179237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.445C>T |
| AA Mutation | p.Arg149Trp(p.R149W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246115 |
| Start | 3179520:3179520(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs566167311 |
| CDS Mutation | c.728G>A |
| AA Mutation | p.Arg243His(p.R243H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246115 |
| Start | 3179651:3179651(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748147679 |
| CDS Mutation | c.859C>T |
| AA Mutation | p.Arg287Trp(p.R287W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246115 |
| Start | 3179133:3179133(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762051085 |
| CDS Mutation | c.341C>T |
| AA Mutation | p.Ala114Val(p.A114V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246115 |
| Start | 3179115:3179115(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.323C>G |
| AA Mutation | p.Ala108Gly(p.A108G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246115 |
| Start | 3179522:3179522(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs768125524 |
| CDS Mutation | c.730C>T |
| AA Mutation | p.Arg244Cys(p.R244C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246115 |
| Start | 3179831:3179831(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369301655 |
| CDS Mutation | c.1039G>A |
| AA Mutation | p.Gly347Arg(p.G347R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000246115 |
| Start | 3179877:3179877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141031634 |
| CDS Mutation | c.1085G>A |
| AA Mutation | p.Arg362His(p.R362H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000246115 |
| Start | 3179080:3179080(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546886910 |
| CDS Mutation | c.288C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000246115 |
| Start | 3179786:3179786(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.994C>T |
| AA Mutation | p.Arg332Ter(p.R332*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |