Primary Site >> Pancreatic Cancer
Gene >> RREB1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349384 |
| Start | 7229035:7229035(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.936G>T |
| AA Mutation | p.Glu312Asp(p.E312D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349384 |
| Start | 7246741:7246741(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4126G>A |
| AA Mutation | p.Glu1376Lys(p.E1376K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349384 |
| Start | 7229646:7229646(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1547G>T |
| AA Mutation | p.Arg516Leu(p.R516L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349384 |
| Start | 7230174:7230174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs756773469 |
| CDS Mutation | c.2075C>T |
| AA Mutation | p.Thr692Met(p.T692M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349384 |
| Start | 7230962:7230962(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs754945001 |
| CDS Mutation | c.2863G>A |
| AA Mutation | p.Glu955Lys(p.E955K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349384 |
| Start | 7229237:7229237(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747673605 |
| CDS Mutation | c.1138G>A |
| AA Mutation | p.Ala380Thr(p.A380T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349384 |
| Start | 7229362:7229362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140980354 |
| CDS Mutation | c.1263C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349384 |
| Start | 7231793:7231793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3694C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349384 |
| Start | 7247085:7247085(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4470C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000349384 |
| Start | 7230337:7230337(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2238delC |
| AA Mutation | p.Asp746GlufsTer167(p.D746Efs*167) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000349384 |
| Start | 7229036:7229036(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.937C>T |
| AA Mutation | p.Gln313Ter(p.Q313*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000349384 |
| Start | 7210877:7210877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.499C>T |
| AA Mutation | p.Arg167Ter(p.R167*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000349384 |
| Start | 7226595:7226596(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.837_838dupTG |
| AA Mutation | p.Gly280ValfsTer6(p.G280Vfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000349384 |
| Start | 7229054:7229055(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.956_959dupACAC |
| AA Mutation | p.Cys321HisfsTer3(p.C321Hfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000349384 |
| Start | 7231555:7231575(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3460_3480delGGCCGGAAAAGGGGGATGAGG |
| AA Mutation | p.Gly1154_Arg1160del(p.G1154_R1160del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |