Primary Site >> Stomach Cancer
Gene >> CUX2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111338403:111338403(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 | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111320681:111320681(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2672A>G |
| AA Mutation | p.Tyr891Cys(p.Y891C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111320518:111320518(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2509G>A |
| AA Mutation | p.Glu837Lys(p.E837K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111312148:111312148(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1949C>T |
| AA Mutation | p.Ala650Val(p.A650V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111320272:111320272(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2263G>A |
| AA Mutation | p.Ala755Thr(p.A755T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111348088:111348088(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4224G>T |
| AA Mutation | p.Met1408Ile(p.M1408I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111341810:111341810(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3416G>A |
| AA Mutation | p.Ser1139Asn(p.S1139N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111347756:111347756(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3892A>G |
| AA Mutation | p.Ile1298Val(p.I1298V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111295341:111295341(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.569A>G |
| AA Mutation | p.Gln190Arg(p.Q190R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111341995:111341995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3601C>A |
| AA Mutation | p.Leu1201Ile(p.L1201I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111214224:111214224(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.88G>C |
| AA Mutation | p.Glu30Gln(p.E30Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111347799:111347799(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3935G>A |
| AA Mutation | p.Gly1312Asp(p.G1312D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111322551:111322551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2897C>T |
| AA Mutation | p.Ala966Val(p.A966V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111310587:111310587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1805C>T |
| AA Mutation | p.Thr602Met(p.T602M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000261726 |
| Start | 111306943:111306943(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.881G>C |
| AA Mutation | p.Cys294Ser(p.C294S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111296519:111296519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.684C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111320349:111320349(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2340C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111291440:111291440(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372659202 |
| CDS Mutation | c.324G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111347824:111347824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3960G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111347608:111347608(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372290639 |
| CDS Mutation | c.3744G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111320622:111320622(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778876224 |
| CDS Mutation | c.2613C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111341976:111341976(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199568145 |
| CDS Mutation | c.3582G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111341814:111341814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376748122 |
| CDS Mutation | c.3420C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111263793:111263793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs547604078 |
| CDS Mutation | c.255G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111293480:111293480(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs750164424 |
| CDS Mutation | c.471G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111320766:111320766(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2757C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111341949:111341949(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200742986 |
| CDS Mutation | c.3555G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000261726 |
| Start | 111307249:111307249(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373896743 |
| CDS Mutation | c.1101G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000261726 |
| Start | 111291501:111291501(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.385C>T |
| AA Mutation | p.Arg129Ter(p.R129*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261726 |
| Start | 111348143:111348144(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs750550645 |
| CDS Mutation | c.4286dupC |
| AA Mutation | p.Ala1430CysfsTer11(p.A1430Cfs*11) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000261726 |
| Start | 111347842:111347843(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.3984dupC |
| AA Mutation | p.Lys1329GlnfsTer10(p.K1329Qfs*10) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | splice_acceptor_variant |
| Transcription ID | ENST00000261726 |
| Start | 111308426:111308426(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1159-1G>T |
| Mutation Classification | Splice_Site |
| Feature Type | Transcript |