Primary Site >> Pancreatic Cancer
Gene >> TGFBR2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295754 |
| Start | 30644881:30644881(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.229T>A |
| AA Mutation | p.Cys77Ser(p.C77S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295754 |
| Start | 30691465:30691465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs727504421 |
| CDS Mutation | c.1570G>T |
| AA Mutation | p.Asp524Tyr(p.D524Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295754 |
| Start | 30672262:30672262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1079A>C |
| AA Mutation | p.His360Pro(p.H360P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295754 |
| Start | 30688458:30688458(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1471G>A |
| AA Mutation | p.Val491Met(p.V491M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295754 |
| Start | 30691478:30691478(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs104893815 |
| CDS Mutation | c.1583G>A |
| AA Mutation | p.Arg528His(p.R528H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295754 |
| Start | 30691472:30691472(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1577A>T |
| AA Mutation | p.Glu526Val(p.E526V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000295754 |
| Start | 30691504:30691504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs104893809 |
| CDS Mutation | c.1609C>T |
| AA Mutation | p.Arg537Cys(p.R537C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000295754 |
| Start | 30672263:30672266(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1081_1084delCTCC |
| AA Mutation | p.Leu361ThrfsTer26(p.L361Tfs*26) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000295754 |
| Start | 30671679:30671679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.496C>T |
| AA Mutation | p.Gln166Ter(p.Q166*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000295754 |
| Start | 30674216:30674216(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1366G>T |
| AA Mutation | p.Glu456Ter(p.E456*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |