Primary Site >> Pancreatic Cancer
Gene >> COL11A1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370096 |
| Start | 102987679:102987679(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749913678 |
| CDS Mutation | c.2456C>G |
| AA Mutation | p.Ala819Gly(p.A819G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370096 |
| Start | 102935109:102935109(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3443C>G |
| AA Mutation | p.Pro1148Arg(p.P1148R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370096 |
| Start | 102962246:102962246(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3044G>C |
| AA Mutation | p.Gly1015Ala(p.G1015A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370096 |
| Start | 102879759:102879759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140250347 |
| CDS Mutation | c.5198G>A |
| AA Mutation | p.Arg1733His(p.R1733H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370096 |
| Start | 103078760:103078760(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.386T>G |
| AA Mutation | p.Val129Gly(p.V129G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370096 |
| Start | 103017870:103017870(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1363C>A |
| AA Mutation | p.Pro455Thr(p.P455T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000370096 |
| Start | 103031191:103031191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.705C>A |
| AA Mutation | p.Tyr235Ter(p.Y235*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |