Primary Site >> Pancreatic Cancer
Gene >> DMBT1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338354 |
| Start | 122643178:122643178(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7022G>A |
| AA Mutation | p.Arg2341His(p.R2341H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338354 |
| Start | 122576654:122576654(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.539G>A |
| AA Mutation | p.Ser180Asn(p.S180N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338354 |
| Start | 122579700:122579700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.802G>T |
| AA Mutation | p.Ala268Ser(p.A268S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338354 |
| Start | 122636008:122636008(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6179A>C |
| AA Mutation | p.Asn2060Thr(p.N2060T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338354 |
| Start | 122629900:122629900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5342C>A |
| AA Mutation | p.Ser1781Tyr(p.S1781Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000338354 |
| Start | 122576564:122576564(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.449C>T |
| AA Mutation | p.Ser150Leu(p.S150L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000338354 |
| Start | 122618067:122618067(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746471340 |
| CDS Mutation | c.4555C>T |
| AA Mutation | p.Arg1519Ter(p.R1519*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000338354 |
| Start | 122573714:122573714(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.236-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |