Primary Site >> Pancreatic Cancer
Gene >> AHNAK
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62517579:62517579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16838T>G |
| AA Mutation | p.Phe5613Cys(p.F5613C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62520461:62520461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.13956G>A |
| AA Mutation | p.Met4652Ile(p.M4652I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62523457:62523457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10960C>A |
| AA Mutation | p.Leu3654Met(p.L3654M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62523868:62523868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10549C>A |
| AA Mutation | p.Leu3517Ile(p.L3517I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62524423:62524423(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9994C>A |
| AA Mutation | p.Pro3332Thr(p.P3332T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62528334:62528334(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772630697 |
| CDS Mutation | c.6083C>T |
| AA Mutation | p.Pro2028Leu(p.P2028L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62531571:62531571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2846C>A |
| AA Mutation | p.Pro949His(p.P949H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62531631:62531631(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2786T>C |
| AA Mutation | p.Leu929Pro(p.L929P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62532051:62532051(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2366C>T |
| AA Mutation | p.Ala789Val(p.A789V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62535965:62535965(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757522801 |
| CDS Mutation | c.134G>A |
| AA Mutation | p.Arg45His(p.R45H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000378024 |
| Start | 62530512:62530512(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs569137878 |
| CDS Mutation | c.3905C>T |
| AA Mutation | p.Pro1302Leu(p.P1302L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378024 |
| Start | 62517413:62517413(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.17004C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378024 |
| Start | 62518283:62518283(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.16134T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378024 |
| Start | 62518346:62518346(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137898001 |
| CDS Mutation | c.16071C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378024 |
| Start | 62519471:62519471(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.14946T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378024 |
| Start | 62526428:62526428(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7989C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378024 |
| Start | 62528588:62528588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs601430 |
| CDS Mutation | c.5829G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378024 |
| Start | 62525846:62525846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8571C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000378024 |
| Start | 62528735:62528735(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5682T>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000378024 |
| Start | 62536048:62536049(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.50dupG |
| AA Mutation | p.Ser18Ter(p.S18*) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |