Primary Site >> Pancreatic Cancer
Gene >> AHNAK2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104941982:104941982(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745381931 |
| CDS Mutation | c.13469C>T |
| AA Mutation | p.Ala4490Val(p.A4490V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104945193:104945193(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10258C>A |
| AA Mutation | p.Leu3420Ile(p.L3420I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946579:104946579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746292166 |
| CDS Mutation | c.8872G>A |
| AA Mutation | p.Ala2958Thr(p.A2958T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104948459:104948459(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6992C>A |
| AA Mutation | p.Ser2331Tyr(p.S2331Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104949840:104949840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374130169 |
| CDS Mutation | c.5611C>A |
| AA Mutation | p.Leu1871Ile(p.L1871I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952311:104952311(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3140G>T |
| AA Mutation | p.Ser1047Ile(p.S1047I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000333244 |
| Start | 104953103:104953103(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2348C>A |
| AA Mutation | p.Pro783His(p.P783H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104954236:104954236(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368999034 |
| CDS Mutation | c.1215C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104940856:104940856(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.14595C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104946424:104946424(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771780782 |
| CDS Mutation | c.9027G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000333244 |
| Start | 104952721:104952721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149453124 |
| CDS Mutation | c.2730C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000333244 |
| Start | 104953956:104953956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1495G>T |
| AA Mutation | p.Glu499Ter(p.E499*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |