Primary Site >> Stomach Cancer
Gene >> TMEM72
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389583 |
| Start | 44935105:44935105(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759085092 |
| CDS Mutation | c.799T>C |
| AA Mutation | p.Ser267Pro(p.S267P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389583 |
| Start | 44934891:44934891(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.585G>T |
| AA Mutation | p.Lys195Asn(p.K195N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389583 |
| Start | 44934722:44934722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.416C>A |
| AA Mutation | p.Ala139Asp(p.A139D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389583 |
| Start | 44934800:44934800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527934388 |
| CDS Mutation | c.494C>T |
| AA Mutation | p.Thr165Ile(p.T165I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389583 |
| Start | 44934725:44934725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.419C>A |
| AA Mutation | p.Pro140His(p.P140H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389583 |
| Start | 44932010:44932010(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80056477 |
| CDS Mutation | c.150C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |