Primary Site >> Stomach Cancer
Gene >> UBASH3A
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319294 |
| Start | 42442497:42442497(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1532T>A |
| AA Mutation | p.Ile511Asn(p.I511N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319294 |
| Start | 42442500:42442500(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1535T>G |
| AA Mutation | p.Phe512Cys(p.F512C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319294 |
| Start | 42409466:42409466(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.212C>A |
| AA Mutation | p.Pro71His(p.P71H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319294 |
| Start | 42443316:42443316(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1636G>A |
| AA Mutation | p.Ala546Thr(p.A546T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319294 |
| Start | 42443346:42443346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs116752327 |
| CDS Mutation | c.1666G>A |
| AA Mutation | p.Glu556Lys(p.E556K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319294 |
| Start | 42437493:42437493(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377495212 |
| CDS Mutation | c.1399G>A |
| AA Mutation | p.Ala467Thr(p.A467T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000319294 |
| Start | 42418594:42418594(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs769032463 |
| CDS Mutation | c.1031C>T |
| AA Mutation | p.Thr344Met(p.T344M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319294 |
| Start | 42437495:42437495(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375005296 |
| CDS Mutation | c.1401G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319294 |
| Start | 42416518:42416518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.744G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319294 |
| Start | 42418463:42418463(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.900T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000319294 |
| Start | 42413185:42413185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750396374 |
| CDS Mutation | c.516C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000319294 |
| Start | 42444582:42444582(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1787delC |
| AA Mutation | p.Thr596SerfsTer19(p.T596Sfs*19) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | stop_gained;frameshift_variant |
| Transcription ID | ENST00000319294 |
| Start | 42418415:42418416(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.852_853insGACCATTTTTACTTATAGATATAGATATAATAATT |
| AA Mutation | p.Phe285AspfsTer6(p.F285Dfs*6) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |