Primary Site >> Pancreatic Cancer
Gene >> IGF2R
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160071931:160071931(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4465A>C |
| AA Mutation | p.Ser1489Arg(p.S1489R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160080134:160080134(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754114803 |
| CDS Mutation | c.5692G>A |
| AA Mutation | p.Asp1898Asn(p.D1898N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160034468:160034468(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1261A>C |
| AA Mutation | p.Ser421Arg(p.S421R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160059017:160059017(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3010C>T |
| AA Mutation | p.Pro1004Ser(p.P1004S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160072819:160072819(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4625A>G |
| AA Mutation | p.Tyr1542Cys(p.Y1542C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000356956 |
| Start | 160075983:160075983(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5303G>A |
| AA Mutation | p.Arg1768Lys(p.R1768K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000356956 |
| Start | 160073289:160073289(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753461516 |
| CDS Mutation | c.4767G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |