Primary Site >> Pancreatic Cancer
Gene >> COL6A2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300527 |
| Start | 46125908:46125908(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2093C>T |
| AA Mutation | p.Ala698Val(p.A698V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300527 |
| Start | 46125288:46125288(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1793T>A |
| AA Mutation | p.Val598Glu(p.V598E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300527 |
| Start | 46132262:46132262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs771749652 |
| CDS Mutation | c.2770G>A |
| AA Mutation | p.Ala924Thr(p.A924T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300527 |
| Start | 46132430:46132430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140020002 |
| CDS Mutation | c.2938G>A |
| AA Mutation | p.Val980Met(p.V980M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300527 |
| Start | 46112405:46112405(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs371640468 |
| CDS Mutation | c.542G>A |
| AA Mutation | p.Arg181His(p.R181H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300527 |
| Start | 46125799:46125799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764497780 |
| CDS Mutation | c.1984G>A |
| AA Mutation | p.Val662Met(p.V662M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000300527 |
| Start | 46118635:46118635(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs142880107 |
| CDS Mutation | c.1138C>T |
| AA Mutation | p.Arg380Cys(p.R380C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300527 |
| Start | 46112419:46112419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.556C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300527 |
| Start | 46112361:46112361(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762436629 |
| CDS Mutation | c.498C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000300527 |
| Start | 46126140:46126140(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs770721679 |
| CDS Mutation | c.2325C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000300527 |
| Start | 46118632:46118632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1135G>T |
| AA Mutation | p.Gly379Ter(p.G379*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |