Primary Site >> Stomach Cancer
Gene >> TRPM5
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000155858 |
| Start | 2415468:2415468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1132T>G |
| AA Mutation | p.Cys378Gly(p.C378G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000155858 |
| Start | 2407769:2407769(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772292156 |
| CDS Mutation | c.2926G>A |
| AA Mutation | p.Ala976Thr(p.A976T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000155858 |
| Start | 2414164:2414164(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1787T>C |
| AA Mutation | p.Phe596Ser(p.F596S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000155858 |
| Start | 2414146:2414146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140559697 |
| CDS Mutation | c.1805G>A |
| AA Mutation | p.Arg602Gln(p.R602Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000155858 |
| Start | 2417753:2417753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763058714 |
| CDS Mutation | c.983C>T |
| AA Mutation | p.Thr328Met(p.T328M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000155858 |
| Start | 2411678:2411678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2564T>A |
| AA Mutation | p.Ile855Lys(p.I855K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000155858 |
| Start | 2415021:2415021(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs752986561 |
| CDS Mutation | c.1506G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000155858 |
| Start | 2415340:2415340(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1260C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000155858 |
| Start | 2420299:2420299(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.572delC |
| AA Mutation | p.Pro191ArgfsTer7(p.P191Rfs*7) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000155858 |
| Start | 2422979:2422979(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.58delG |
| AA Mutation | p.Glu20SerfsTer61(p.E20Sfs*61) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000155858 |
| Start | 2406060:2406061(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3282_3283insG |
| AA Mutation | p.Leu1095AlafsTer27(p.L1095Afs*27) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |