Primary Site >> Stomach Cancer
Gene >> LPL
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311322 |
| Start | 19954191:19954191(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.613T>G |
| AA Mutation | p.Phe205Val(p.F205V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311322 |
| Start | 19959300:19959300(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747267560 |
| CDS Mutation | c.1059G>C |
| AA Mutation | p.Glu353Asp(p.E353D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311322 |
| Start | 19954329:19954329(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs377128614 |
| CDS Mutation | c.751G>A |
| AA Mutation | p.Val251Met(p.V251M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311322 |
| Start | 19953388:19953388(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.508A>C |
| AA Mutation | p.Ser170Arg(p.S170R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311322 |
| Start | 19961037:19961037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1276T>C |
| AA Mutation | p.Phe426Leu(p.F426L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311322 |
| Start | 19948314:19948314(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.223A>G |
| AA Mutation | p.Thr75Ala(p.T75A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000311322 |
| Start | 19951928:19951928(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376875031 |
| CDS Mutation | c.409C>T |
| AA Mutation | p.Arg137Trp(p.R137W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311322 |
| Start | 19955893:19955893(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766760812 |
| CDS Mutation | c.828C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000311322 |
| Start | 19948196:19948196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145405273 |
| CDS Mutation | c.105C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |