Primary Site >> Stomach Cancer
Gene >> TAS1R3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339381 |
| Start | 1332781:1332781(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1250C>T |
| AA Mutation | p.Ala417Val(p.A417V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339381 |
| Start | 1333088:1333088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1443G>T |
| AA Mutation | p.Glu481Asp(p.E481D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339381 |
| Start | 1331684:1331684(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371880423 |
| CDS Mutation | c.238G>A |
| AA Mutation | p.Val80Met(p.V80M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339381 |
| Start | 1331715:1331715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.269T>C |
| AA Mutation | p.Leu90Pro(p.L90P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339381 |
| Start | 1332717:1332717(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1186G>A |
| AA Mutation | p.Ala396Thr(p.A396T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000339381 |
| Start | 1331461:1331461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs577691125 |
| CDS Mutation | c.116G>A |
| AA Mutation | p.Gly39Glu(p.G39E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339381 |
| Start | 1332776:1332776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs761662561 |
| CDS Mutation | c.1245C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339381 |
| Start | 1334431:1334431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2526C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339381 |
| Start | 1332458:1332458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.927C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000339381 |
| Start | 1332977:1332977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1332C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000339381 |
| Start | 1333711:1333711(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs777573279 |
| CDS Mutation | c.1812delG |
| AA Mutation | p.Leu606TrpfsTer43(p.L606Wfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000339381 |
| Start | 1331407:1331407(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.65delC |
| AA Mutation | p.Pro22HisfsTer10(p.P22Hfs*10) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000339381 |
| Start | 1333718:1333718(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1816delC |
| AA Mutation | p.Leu606TrpfsTer43(p.L606Wfs*43) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000339381 |
| Start | 1331455:1331456(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs760227174 |
| CDS Mutation | c.117dupG |
| AA Mutation | p.Leu40AlafsTer62(p.L40Afs*62) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |