Primary Site >> Pancreatic Cancer
Gene >> PLEKHG2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425673 |
| Start | 39418036:39418036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1014C>A |
| AA Mutation | p.Phe338Leu(p.F338L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425673 |
| Start | 39416971:39416971(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.715C>T |
| AA Mutation | p.Arg239Cys(p.R239C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000425673 |
| Start | 39418051:39418051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1029G>T |
| AA Mutation | p.Met343Ile(p.M343I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000425673 |
| Start | 39416956:39416956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.700C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000425673 |
| Start | 39424231:39424231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3098C>G |
| AA Mutation | p.Ser1033Ter(p.S1033*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000425673 |
| Start | 39415344:39415344(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.384C>A |
| AA Mutation | p.Tyr128Ter(p.Y128*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |