Primary Site >> Pancreatic Cancer
Gene >> ADAMTS20
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389420 |
| Start | 43492595:43492595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.986C>T |
| AA Mutation | p.Thr329Ile(p.T329I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389420 |
| Start | 43453944:43453944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150619594 |
| CDS Mutation | c.1723G>A |
| AA Mutation | p.Gly575Arg(p.G575R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389420 |
| Start | 43425525:43425525(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4273C>A |
| AA Mutation | p.Pro1425Thr(p.P1425T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389420 |
| Start | 43383623:43383623(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4732C>A |
| AA Mutation | p.Leu1578Ile(p.L1578I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389420 |
| Start | 43492586:43492586(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375762593 |
| CDS Mutation | c.995A>C |
| AA Mutation | p.Asn332Thr(p.N332T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389420 |
| Start | 43466789:43466789(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1230T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |