Primary Site >> Pancreatic Cancer
Gene >> PLEC
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143917804:143917804(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200521669 |
| CDS Mutation | c.12428C>T |
| AA Mutation | p.Ser4143Leu(p.S4143L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143919929:143919929(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.10303C>A |
| AA Mutation | p.Leu3435Met(p.L3435M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143917537:143917537(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12695C>T |
| AA Mutation | p.Thr4232Met(p.T4232M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143918830:143918830(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782426059 |
| CDS Mutation | c.11402A>G |
| AA Mutation | p.Asn3801Ser(p.N3801S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143920795:143920795(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9437A>G |
| AA Mutation | p.Asp3146Gly(p.D3146G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143921405:143921405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8827C>A |
| AA Mutation | p.Leu2943Met(p.L2943M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143923172:143923172(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs62641756 |
| CDS Mutation | c.7168G>A |
| AA Mutation | p.Ala2390Thr(p.A2390T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143923229:143923229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782319175 |
| CDS Mutation | c.7111C>T |
| AA Mutation | p.Arg2371Cys(p.R2371C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143930158:143930158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3009G>T |
| AA Mutation | p.Gln1003His(p.Q1003H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143932923:143932923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2018A>C |
| AA Mutation | p.Gln673Pro(p.Q673P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143934355:143934355(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1543C>A |
| AA Mutation | p.Leu515Met(p.L515M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143922302:143922302(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782503698 |
| CDS Mutation | c.7930C>T |
| AA Mutation | p.Arg2644Cys(p.R2644C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000322810 |
| Start | 143917915:143917915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782096389 |
| CDS Mutation | c.12317C>T |
| AA Mutation | p.Ala4106Val(p.A4106V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322810 |
| Start | 143917941:143917941(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.12291C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322810 |
| Start | 143917041:143917041(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782590185 |
| CDS Mutation | c.13191C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322810 |
| Start | 143917377:143917377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143548638 |
| CDS Mutation | c.12855G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322810 |
| Start | 143917431:143917431(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200575172 |
| CDS Mutation | c.12801G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322810 |
| Start | 143921693:143921693(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8539C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322810 |
| Start | 143921760:143921760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs542710594 |
| CDS Mutation | c.8472C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322810 |
| Start | 143923530:143923530(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375489890 |
| CDS Mutation | c.6810G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000322810 |
| Start | 143933343:143933343(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1683G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000322810 |
| Start | 143927510:143927510(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4067delT |
| AA Mutation | p.Leu1356TrpfsTer69(p.L1356Wfs*69) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000322810 |
| Start | 143920817:143920817(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs137853161 |
| CDS Mutation | c.9415C>T |
| AA Mutation | p.Arg3139Ter(p.R3139*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000322810 |
| Start | 143922653:143922653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7687G>T |
| AA Mutation | p.Glu2563Ter(p.E2563*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |