Primary Site >> Stomach Cancer
Gene >> LMBRD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69700796:69700796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs772350306 |
| CDS Mutation | c.1157G>A |
| AA Mutation | p.Arg386Gln(p.R386Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69713758:69713758(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs143758103 |
| CDS Mutation | c.802G>A |
| AA Mutation | p.Ala268Thr(p.A268T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69713656:69713656(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376456203 |
| CDS Mutation | c.904C>T |
| AA Mutation | p.Arg302Cys(p.R302C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69697638:69697638(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1342A>G |
| AA Mutation | p.Asn448Asp(p.N448D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69713730:69713730(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs747354714 |
| CDS Mutation | c.830G>A |
| AA Mutation | p.Arg277Gln(p.R277Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69749362:69749362(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.452G>T |
| AA Mutation | p.Cys151Phe(p.C151F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69719071:69719071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.647T>C |
| AA Mutation | p.Met216Thr(p.M216T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69790319:69790319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.223A>G |
| AA Mutation | p.Lys75Glu(p.K75E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69699146:69699146(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1235T>G |
| AA Mutation | p.Phe412Cys(p.F412C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69780511:69780511(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.290T>C |
| AA Mutation | p.Val97Ala(p.V97A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000370577 |
| Start | 69713755:69713755(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.805T>G |
| AA Mutation | p.Leu269Val(p.L269V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370577 |
| Start | 69719004:69719004(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.714T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000370577 |
| Start | 69713663:69713663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757392138 |
| CDS Mutation | c.897C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370577 |
| Start | 69790385:69790385(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.157delT |
| AA Mutation | p.Ser53LeufsTer2(p.S53Lfs*2) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000370577 |
| Start | 69790464:69790465(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.77dupT |
| AA Mutation | p.Leu26PhefsTer10(p.L26Ffs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |