Primary Site >> Pancreatic Cancer
Gene >> LCT
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809879:135809879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2468G>A |
| AA Mutation | p.Ser823Asn(p.S823N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809667:135809667(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777321408 |
| CDS Mutation | c.2680G>A |
| AA Mutation | p.Glu894Lys(p.E894K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264162 |
| Start | 135812385:135812385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2279G>A |
| AA Mutation | p.Gly760Glu(p.G760E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135809935:135809935(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2412C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135812507:135812507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2157G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264162 |
| Start | 135836738:135836738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774168782 |
| CDS Mutation | c.432C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264162 |
| Start | 135807370:135807370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3931C>T |
| AA Mutation | p.Arg1311Ter(p.R1311*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000264162 |
| Start | 135817523:135817523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1525G>T |
| AA Mutation | p.Gly509Ter(p.G509*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |