Primary Site >> Stomach Cancer
Gene >> LRRC15
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347624 |
| Start | 194360158:194360158(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs180967725 |
| CDS Mutation | c.886C>T |
| AA Mutation | p.Arg296Trp(p.R296W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347624 |
| Start | 194360014:194360014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373653527 |
| CDS Mutation | c.1030C>T |
| AA Mutation | p.Arg344Trp(p.R344W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347624 |
| Start | 194360013:194360013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767913133 |
| CDS Mutation | c.1031G>A |
| AA Mutation | p.Arg344Gln(p.R344Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347624 |
| Start | 194360211:194360211(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748458933 |
| CDS Mutation | c.833G>A |
| AA Mutation | p.Gly278Glu(p.G278E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347624 |
| Start | 194359417:194359417(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774070397 |
| CDS Mutation | c.1627G>A |
| AA Mutation | p.Ala543Thr(p.A543T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000347624 |
| Start | 194359824:194359824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1220G>A |
| AA Mutation | p.Gly407Asp(p.G407D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347624 |
| Start | 194359418:194359418(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs113394891 |
| CDS Mutation | c.1626C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347624 |
| Start | 194359973:194359973(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369755501 |
| CDS Mutation | c.1071C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347624 |
| Start | 194360492:194360492(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779197120 |
| CDS Mutation | c.552C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000347624 |
| Start | 194359370:194359370(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200049182 |
| CDS Mutation | c.1674C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000347624 |
| Start | 194360187:194360188(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.856_857delCC |
| AA Mutation | p.Pro286GlyfsTer16(p.P286Gfs*16) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |