Primary Site >> Stomach Cancer
Gene >> UBA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335972 |
| Start | 47211208:47211208(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2447G>A |
| AA Mutation | p.Ser816Asn(p.S816N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335972 |
| Start | 47206266:47206266(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1760G>A |
| AA Mutation | p.Arg587His(p.R587H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335972 |
| Start | 47213167:47213167(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2824G>A |
| AA Mutation | p.Ala942Thr(p.A942T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335972 |
| Start | 47201561:47201561(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.762G>T |
| AA Mutation | p.Gln254His(p.Q254H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335972 |
| Start | 47199217:47199217(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.185T>C |
| AA Mutation | p.Leu62Ser(p.L62S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000335972 |
| Start | 47202365:47202365(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.917T>C |
| AA Mutation | p.Leu306Ser(p.L306S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335972 |
| Start | 47202196:47202196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781839047 |
| CDS Mutation | c.852C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000335972 |
| Start | 47203151:47203151(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375669736 |
| CDS Mutation | c.1356C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | splice_acceptor_variant;intron_variant |
| Transcription ID | ENST00000335972 |
| Start | 47202148:47202155(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.812-8_812-1delCTCTGTAG |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |