Primary Site >> Stomach Cancer
Gene >> LGR6
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367278 |
| Start | 202319143:202319143(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2840G>A |
| AA Mutation | p.Gly947Asp(p.G947D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367278 |
| Start | 202280827:202280827(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs546447981 |
| CDS Mutation | c.691G>A |
| AA Mutation | p.Glu231Lys(p.E231K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367278 |
| Start | 202318723:202318723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2420C>A |
| AA Mutation | p.Ala807Asp(p.A807D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367278 |
| Start | 202319014:202319014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2711G>A |
| AA Mutation | p.Cys904Tyr(p.C904Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367278 |
| Start | 202318064:202318064(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1761C>G |
| AA Mutation | p.Phe587Leu(p.F587L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367278 |
| Start | 202318708:202318708(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2405C>A |
| AA Mutation | p.Pro802His(p.P802H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367278 |
| Start | 202194194:202194194(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.205G>A |
| AA Mutation | p.Ala69Thr(p.A69T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367278 |
| Start | 202318131:202318131(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1828T>A |
| AA Mutation | p.Leu610Met(p.L610M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367278 |
| Start | 202306923:202306923(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1192A>G |
| AA Mutation | p.Ser398Gly(p.S398G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000367278 |
| Start | 202300874:202300874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.811G>A |
| AA Mutation | p.Ala271Thr(p.A271T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367278 |
| Start | 202318184:202318184(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1881T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367278 |
| Start | 202307345:202307345(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs146190126 |
| CDS Mutation | c.1224C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000367278 |
| Start | 202318625:202318625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199692167 |
| CDS Mutation | c.2322C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367278 |
| Start | 202319029:202319029(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2730delC |
| AA Mutation | p.Arg911GlyfsTer8(p.R911Gfs*8) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000367278 |
| Start | 202319157:202319157(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2858delG |
| AA Mutation | p.Gly953ValfsTer35(p.G953Vfs*35) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000367278 |
| Start | 202317951:202317951(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1649-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |