Primary Site >> Stomach Cancer
Gene >> UTS2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361696 |
| Start | 7847851:7847851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.290T>G |
| AA Mutation | p.Ile97Ser(p.I97S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361696 |
| Start | 7847842:7847842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.299G>T |
| AA Mutation | p.Ser100Ile(p.S100I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361696 |
| Start | 7852977:7852977(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.27G>T |
| AA Mutation | p.Leu9Phe(p.L9F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361696 |
| Start | 7850905:7850905(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs776604807 |
| CDS Mutation | c.121C>T |
| AA Mutation | p.Arg41Cys(p.R41C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000361696 |
| Start | 7850908:7850908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201977733 |
| CDS Mutation | c.118G>A |
| AA Mutation | p.Ala40Thr(p.A40T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000361696 |
| Start | 7852978:7852979(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.25_26insAATA |
| AA Mutation | p.Leu9Ter(p.L9*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |