Primary Site >> Stomach Cancer
Gene >> LDLR
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558518 |
| Start | 11113338:11113338(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs773658037 |
| CDS Mutation | c.1247G>A |
| AA Mutation | p.Arg416Gln(p.R416Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558518 |
| Start | 11106579:11106579(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.709C>T |
| AA Mutation | p.Arg237Cys(p.R237C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558518 |
| Start | 11105507:11105507(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.601G>A |
| AA Mutation | p.Glu201Lys(p.E201K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558518 |
| Start | 11102715:11102715(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.242G>A |
| AA Mutation | p.Arg81His(p.R81H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558518 |
| Start | 11113722:11113722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141673997 |
| CDS Mutation | c.1546G>A |
| AA Mutation | p.Gly516Ser(p.G516S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558518 |
| Start | 11113292:11113292(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1201C>A |
| AA Mutation | p.Leu401Ile(p.L401I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558518 |
| Start | 11102706:11102706(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146675823 |
| CDS Mutation | c.233G>A |
| AA Mutation | p.Arg78His(p.R78H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000558518 |
| Start | 11107514:11107514(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs72658858 |
| CDS Mutation | c.940G>A |
| AA Mutation | p.Gly314Arg(p.G314R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000558518 |
| Start | 11113392:11113392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745343524 |
| CDS Mutation | c.1301C>T |
| AA Mutation | p.Thr434Met(p.T434M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558518 |
| Start | 11123229:11123229(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2196C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558518 |
| Start | 11120437:11120437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149126953 |
| CDS Mutation | c.2055G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558518 |
| Start | 11105572:11105572(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.666C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558518 |
| Start | 11131307:11131307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139757711 |
| CDS Mutation | c.2574C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558518 |
| Start | 11105470:11105470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs121908034 |
| CDS Mutation | c.564C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558518 |
| Start | 11102740:11102740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs777640882 |
| CDS Mutation | c.267C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558518 |
| Start | 11113375:11113375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368708058 |
| CDS Mutation | c.1284C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000558518 |
| Start | 11110704:11110704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147905921 |
| CDS Mutation | c.993C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |