Primary Site >> Stomach Cancer
Gene >> LRP8
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306052 |
| Start | 53258432:53258432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2096G>A |
| AA Mutation | p.Gly699Asp(p.G699D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306052 |
| Start | 53264214:53264214(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150845542 |
| CDS Mutation | c.1610G>A |
| AA Mutation | p.Arg537His(p.R537H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306052 |
| Start | 53262192:53262192(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767691715 |
| CDS Mutation | c.1790G>A |
| AA Mutation | p.Arg597His(p.R597H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000306052 |
| Start | 53255117:53255117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753134602 |
| CDS Mutation | c.2503G>A |
| AA Mutation | p.Val835Met(p.V835M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306052 |
| Start | 53262506:53262506(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1714G>A |
| AA Mutation | p.Gly572Ser(p.G572S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306052 |
| Start | 53249414:53249414(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2819A>G |
| AA Mutation | p.Asn940Ser(p.N940S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306052 |
| Start | 53247025:53247025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2885T>C |
| AA Mutation | p.Leu962Pro(p.L962P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306052 |
| Start | 53262457:53262457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1763G>A |
| AA Mutation | p.Gly588Glu(p.G588E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000306052 |
| Start | 53264250:53264250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1574C>T |
| AA Mutation | p.Thr525Ile(p.T525I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306052 |
| Start | 53262188:53262188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1794G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306052 |
| Start | 53255145:53255145(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146836225 |
| CDS Mutation | c.2475C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306052 |
| Start | 53275731:53275731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757325426 |
| CDS Mutation | c.906C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306052 |
| Start | 53249419:53249419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145707126 |
| CDS Mutation | c.2814G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000306052 |
| Start | 53266610:53266610(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs139974918 |
| CDS Mutation | c.1290C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |