Primary Site >> Stomach Cancer
Gene >> NOTCH2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119916013:119916013(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6709A>T |
| AA Mutation | p.Ser2237Cys(p.S2237C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119950777:119950777(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2426C>A |
| AA Mutation | p.Thr809Asn(p.T809N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119997089:119997089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.659G>A |
| AA Mutation | p.Ser220Asn(p.S220N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119920357:119920357(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5351T>A |
| AA Mutation | p.Ile1784Asn(p.I1784N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119923772:119923772(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4724C>T |
| AA Mutation | p.Thr1575Ile(p.T1575I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119925461:119925461(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4355G>T |
| AA Mutation | p.Gly1452Val(p.G1452V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119963724:119963724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1765G>A |
| AA Mutation | p.Asp589Asn(p.D589N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119950824:119950824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2379G>T |
| AA Mutation | p.Gln793His(p.Q793H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119915385:119915385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375049462 |
| CDS Mutation | c.7337G>T |
| AA Mutation | p.Gly2446Val(p.G2446V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119937367:119937367(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3437G>A |
| AA Mutation | p.Cys1146Tyr(p.C1146Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119922750:119922750(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4888C>T |
| AA Mutation | p.Arg1630Cys(p.R1630C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119937430:119937430(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3374T>G |
| AA Mutation | p.Val1125Gly(p.V1125G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119955215:119955215(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2044G>C |
| AA Mutation | p.Asp682His(p.D682H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119937989:119937989(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61752485 |
| CDS Mutation | c.3205C>T |
| AA Mutation | p.Arg1069Trp(p.R1069W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119997287:119997287(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.461C>T |
| AA Mutation | p.Ala154Val(p.A154V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119919323:119919323(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5770G>T |
| AA Mutation | p.Gly1924Cys(p.G1924C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119929089:119929089(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs75423398 |
| CDS Mutation | c.3779G>A |
| AA Mutation | p.Arg1260His(p.R1260H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119935529:119935529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3598G>T |
| AA Mutation | p.Gly1200Cys(p.G1200C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119963672:119963672(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1817A>G |
| AA Mutation | p.Asp606Gly(p.D606G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119986980:119986980(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782452794 |
| CDS Mutation | c.854G>A |
| AA Mutation | p.Arg285His(p.R285H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119919436:119919436(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5657G>A |
| AA Mutation | p.Arg1886His(p.R1886H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119916054:119916054(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6668A>G |
| AA Mutation | p.Gln2223Arg(p.Q2223R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 120005529:120005529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs201838650 |
| CDS Mutation | c.215G>A |
| AA Mutation | p.Arg72His(p.R72H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119920309:119920309(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5399G>A |
| AA Mutation | p.Arg1800His(p.R1800H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119919454:119919454(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5639C>T |
| AA Mutation | p.Ala1880Val(p.A1880V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119940622:119940622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs61755044 |
| CDS Mutation | c.3116C>T |
| AA Mutation | p.Thr1039Met(p.T1039M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119922297:119922297(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5152C>T |
| AA Mutation | p.Arg1718Cys(p.R1718C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000256646 |
| Start | 119997150:119997150(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.598A>G |
| AA Mutation | p.Asn200Asp(p.N200D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256646 |
| Start | 119916245:119916245(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145566650 |
| CDS Mutation | c.6477G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256646 |
| Start | 119941663:119941663(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2844A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256646 |
| Start | 119937885:119937885(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3309C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256646 |
| Start | 119955132:119955132(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs141051853 |
| CDS Mutation | c.2127C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256646 |
| Start | 119997097:119997097(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs150410907 |
| CDS Mutation | c.651C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000256646 |
| Start | 119922709:119922709(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs587697719 |
| CDS Mutation | c.4929G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256646 |
| Start | 119937948:119937948(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.3246delA |
| AA Mutation | p.Ala1083GlnfsTer25(p.A1083Qfs*25) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000256646 |
| Start | 119968149:119968149(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1192C>T |
| AA Mutation | p.Gln398Ter(p.Q398*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000256646 |
| Start | 119919581:119919581(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs766543218 |
| CDS Mutation | c.5512C>T |
| AA Mutation | p.Arg1838Ter(p.R1838*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256646 |
| Start | 119916014:119916015(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.6707_6708insT |
| AA Mutation | p.Ser2237GlnfsTer7(p.S2237Qfs*7) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000256646 |
| Start | 119997226:119997227(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.521dupT |
| AA Mutation | p.Thr175HisfsTer6(p.T175Hfs*6) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |