Primary Site >> Pancreatic Cancer
Gene >> PEG3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56816649:56816649(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767339103 |
| CDS Mutation | c.1793G>A |
| AA Mutation | p.Arg598His(p.R598H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56817538:56817538(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771139564 |
| CDS Mutation | c.904C>T |
| AA Mutation | p.Arg302Trp(p.R302W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56815653:56815653(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200205197 |
| CDS Mutation | c.2789G>A |
| AA Mutation | p.Arg930His(p.R930H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56817180:56817180(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1262A>G |
| AA Mutation | p.Glu421Gly(p.E421G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56824281:56824281(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.375G>T |
| AA Mutation | p.Lys125Asn(p.K125N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56813775:56813775(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4667C>A |
| AA Mutation | p.Ala1556Asp(p.A1556D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56816007:56816007(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2435C>T |
| AA Mutation | p.Ala812Val(p.A812V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56816815:56816815(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1627G>A |
| AA Mutation | p.Ala543Thr(p.A543T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56817123:56817123(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1319C>T |
| AA Mutation | p.Thr440Ile(p.T440I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56817322:56817322(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1120G>A |
| AA Mutation | p.Gly374Ser(p.G374S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000326441 |
| Start | 56821718:56821718(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139872811 |
| CDS Mutation | c.602C>T |
| AA Mutation | p.Ala201Val(p.A201V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000326441 |
| Start | 56823663:56823663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146592671 |
| CDS Mutation | c.411C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |