Primary Site >> Stomach Cancer
Gene >> SMARCC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267064 |
| Start | 56186200:56186200(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.272G>T |
| AA Mutation | p.Cys91Phe(p.C91F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267064 |
| Start | 56178515:56178515(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200931713 |
| CDS Mutation | c.1199C>T |
| AA Mutation | p.Thr400Met(p.T400M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267064 |
| Start | 56174688:56174688(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1459C>T |
| AA Mutation | p.Arg487Cys(p.R487C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267064 |
| Start | 56169643:56169643(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2508G>T |
| AA Mutation | p.Lys836Asn(p.K836N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267064 |
| Start | 56186207:56186207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.265T>C |
| AA Mutation | p.Ser89Pro(p.S89P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267064 |
| Start | 56172465:56172465(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1796G>A |
| AA Mutation | p.Arg599His(p.R599H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267064 |
| Start | 56181006:56181006(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1052A>G |
| AA Mutation | p.Asn351Ser(p.N351S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267064 |
| Start | 56171871:56171871(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1900G>A |
| AA Mutation | p.Glu634Lys(p.E634K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267064 |
| Start | 56168114:56168114(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2703C>G |
| AA Mutation | p.Ile901Met(p.I901M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000267064 |
| Start | 56173800:56173800(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1546G>C |
| AA Mutation | p.Ala516Pro(p.A516P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267064 |
| Start | 56171722:56171722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2049C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267064 |
| Start | 56169571:56169571(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781082341 |
| CDS Mutation | c.2580C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267064 |
| Start | 56165337:56165337(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3120T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267064 |
| Start | 56178427:56178427(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753819378 |
| CDS Mutation | c.1287C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267064 |
| Start | 56181592:56181592(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.846C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267064 |
| Start | 56165618:56165618(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2839C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267064 |
| Start | 56171932:56171932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1839G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267064 |
| Start | 56169801:56169801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs148688009 |
| CDS Mutation | c.2430C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000267064 |
| Start | 56187262:56187262(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.156G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000267064 |
| Start | 56165329:56165329(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs760211512 |
| CDS Mutation | c.3128delC |
| AA Mutation | p.Pro1043LeufsTer18(p.P1043Lfs*18) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000267064 |
| Start | 56164581:56164642(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3229_3290delGCTCCTTTGGGTTTGCCTTTTGGCATGCCGCCTCCTCCTCCTCCTCCTGCTCCATCCATCAT |
| AA Mutation | p.Ala1077ProfsTer4(p.A1077Pfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000267064 |
| Start | 56163751:56163751(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3583delC |
| AA Mutation | p.Leu1195CysfsTer88(p.L1195Cfs*88) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | stop_gained;splice_region_variant |
| Transcription ID | ENST00000267064 |
| Start | 56185111:56185111(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.318G>A |
| AA Mutation | p.Trp106Ter(p.W106*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000267064 |
| Start | 56169807:56169809(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2422_2424delAAG |
| AA Mutation | p.Lys808del(p.K808del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |