Primary Site >> Stomach Cancer
Gene >> CTNNA2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 79858025:79858025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.311G>A |
| AA Mutation | p.Arg104Gln(p.R104Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80555846:80555846(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1694T>G |
| AA Mutation | p.Val565Gly(p.V565G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80419570:80419570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1259T>C |
| AA Mutation | p.Val420Ala(p.V420A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 79651589:79651589(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.33A>T |
| AA Mutation | p.Lys11Asn(p.K11N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 79858073:79858073(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751827909 |
| CDS Mutation | c.359G>A |
| AA Mutation | p.Arg120His(p.R120H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80604163:80604163(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2279G>A |
| AA Mutation | p.Arg760His(p.R760H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80574307:80574307(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1886T>C |
| AA Mutation | p.Met629Thr(p.M629T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80581814:80581814(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs764740838 |
| CDS Mutation | c.2002G>A |
| AA Mutation | p.Ala668Thr(p.A668T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80545915:80545915(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1392T>A |
| AA Mutation | p.Asn464Lys(p.N464K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80647748:80647748(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2738A>C |
| AA Mutation | p.Lys913Thr(p.K913T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80419570:80419570(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1259T>G |
| AA Mutation | p.Val420Gly(p.V420G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 79909723:79909723(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.982C>T |
| AA Mutation | p.Arg328Cys(p.R328C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80608190:80608190(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2302G>T |
| AA Mutation | p.Asp768Tyr(p.D768Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 79909782:79909782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1041C>G |
| AA Mutation | p.Ser347Arg(p.S347R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80545925:80545925(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1402A>C |
| AA Mutation | p.Thr468Pro(p.T468P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 79858060:79858060(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.346T>A |
| AA Mutation | p.Ser116Thr(p.S116T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80581754:80581754(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1942G>T |
| AA Mutation | p.Asp648Tyr(p.D648Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80574279:80574279(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765711976 |
| CDS Mutation | c.1858G>A |
| AA Mutation | p.Val620Ile(p.V620I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 79909673:79909673(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.932T>C |
| AA Mutation | p.Ile311Thr(p.I311T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80647724:80647724(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2714C>T |
| AA Mutation | p.Ser905Phe(p.S905F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80589389:80589389(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2093A>C |
| AA Mutation | p.Asp698Ala(p.D698A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000402739 |
| Start | 80604174:80604174(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2290G>T |
| AA Mutation | p.Asp764Tyr(p.D764Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 79869927:79869927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.577A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 80419481:80419481(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1170C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 80608225:80608225(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2337T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 79909782:79909782(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1041C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 80546020:80546020(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs200693218 |
| CDS Mutation | c.1497C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 79909710:79909710(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.969G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 79909740:79909740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.999G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 80608294:80608294(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2406G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 79858029:79858029(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs536540906 |
| CDS Mutation | c.315C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 80647624:80647624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2614C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 79869860:79869860(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.510A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 79858062:79858062(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs759308198 |
| CDS Mutation | c.348G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 79874207:79874207(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751210708 |
| CDS Mutation | c.717C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 80419568:80419568(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1257A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000402739 |
| Start | 79909722:79909722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs745441744 |
| CDS Mutation | c.981G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000402739 |
| Start | 80419567:80419568(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.1256_1257delAA |
| AA Mutation | p.Gln419ArgfsTer4(p.Q419Rfs*4) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000402739 |
| Start | 80589422:80589424(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2128_2130delGAT |
| AA Mutation | p.Asp710del(p.D710del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | protein_altering_variant |
| Transcription ID | ENST00000402739 |
| Start | 79858129:79858130(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.416_417insGCCTGT |
| AA Mutation | p.Ile139delinsMetProVal(p.I139delinsMPV) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |