Primary Site >> Stomach Cancer
Gene >> SMARCA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2086916:2086916(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2614G>A |
| AA Mutation | p.Val872Met(p.V872M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2097391:2097391(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2998G>A |
| AA Mutation | p.Gly1000Arg(p.G1000R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2123753:2123753(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3797G>A |
| AA Mutation | p.Arg1266Gln(p.R1266Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2039502:2039502(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.392C>A |
| AA Mutation | p.Pro131Gln(p.P131Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2054701:2054701(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1151G>A |
| AA Mutation | p.Arg384Gln(p.R384Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2123835:2123835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3879G>T |
| AA Mutation | p.Arg1293Ser(p.R1293S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2086906:2086906(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2604C>A |
| AA Mutation | p.Asn868Lys(p.N868K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2032958:2032958(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs762444118 |
| CDS Mutation | c.232G>A |
| AA Mutation | p.Asp78Asn(p.D78N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2056757:2056757(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1259G>A |
| AA Mutation | p.Arg420His(p.R420H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2104047:2104047(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779591664 |
| CDS Mutation | c.3170G>A |
| AA Mutation | p.Arg1057His(p.R1057H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2039604:2039604(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.494G>A |
| AA Mutation | p.Ser165Asn(p.S165N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2086956:2086956(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2654A>G |
| AA Mutation | p.Gln885Arg(p.Q885R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2110275:2110275(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3314G>A |
| AA Mutation | p.Arg1105His(p.R1105H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2060967:2060967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1673A>G |
| AA Mutation | p.Lys558Arg(p.K558R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2056835:2056835(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1337A>G |
| AA Mutation | p.Gln446Arg(p.Q446R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2054682:2054682(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs753807887 |
| CDS Mutation | c.1132G>T |
| AA Mutation | p.Val378Leu(p.V378L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2104016:2104016(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3139C>T |
| AA Mutation | p.Arg1047Trp(p.R1047W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2084171:2084171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2501T>C |
| AA Mutation | p.Ile834Thr(p.I834T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2039678:2039678(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.568A>G |
| AA Mutation | p.Lys190Glu(p.K190E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2191331:2191331(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4660G>T |
| AA Mutation | p.Gly1554Cys(p.G1554C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2161782:2161782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4078G>A |
| AA Mutation | p.Asp1360Asn(p.D1360N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2161854:2161854(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4150A>G |
| AA Mutation | p.Thr1384Ala(p.T1384A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2073576:2073576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1888G>T |
| AA Mutation | p.Ala630Ser(p.A630S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2161726:2161726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4022T>C |
| AA Mutation | p.Val1341Ala(p.V1341A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000349721 |
| Start | 2058432:2058432(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1489C>T |
| AA Mutation | p.Arg497Trp(p.R497W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349721 |
| Start | 2084121:2084121(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2451G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349721 |
| Start | 2123796:2123796(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764977538 |
| CDS Mutation | c.3840G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349721 |
| Start | 2182188:2182188(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4407G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349721 |
| Start | 2076291:2076291(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765966954 |
| CDS Mutation | c.1998C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349721 |
| Start | 2123850:2123850(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141291951 |
| CDS Mutation | c.3894A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000349721 |
| Start | 2161877:2161877(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763381660 |
| CDS Mutation | c.4173C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000349721 |
| Start | 2181665:2181665(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.4354delA |
| AA Mutation | p.Ile1452Ter(p.I1452*) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000349721 |
| Start | 2033024:2033024(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.298C>T |
| AA Mutation | p.Arg100Ter(p.R100*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000349721 |
| Start | 2047441:2047441(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1003C>T |
| AA Mutation | p.Gln335Ter(p.Q335*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |