Primary Site >> Pancreatic Cancer
Gene >> LAMA1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7032157:7032157(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745529420 |
| CDS Mutation | c.2183A>G |
| AA Mutation | p.Tyr728Cys(p.Y728C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7023335:7023335(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369294134 |
| CDS Mutation | c.2530G>A |
| AA Mutation | p.Glu844Lys(p.E844K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6943389:6943389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.8858T>C |
| AA Mutation | p.Val2953Ala(p.V2953A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6947174:6947174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8833G>A |
| AA Mutation | p.Val2945Met(p.V2945M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6948456:6948456(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.8657A>G |
| AA Mutation | p.Tyr2886Cys(p.Y2886C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6973185:6973185(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6646A>G |
| AA Mutation | p.Ser2216Gly(p.S2216G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7034542:7034542(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1988T>C |
| AA Mutation | p.Leu663Pro(p.L663P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 6943189:6943189(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.9058G>A |
| AA Mutation | p.Gly3020Ser(p.G3020S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000389658 |
| Start | 7036030:7036030(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148234507 |
| CDS Mutation | c.1796C>T |
| AA Mutation | p.Thr599Met(p.T599M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000389658 |
| Start | 7013956:7013956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760611120 |
| CDS Mutation | c.3222C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |