Primary Site >> Stomach Cancer
Gene >> CTNND2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11022802:11022802(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2966A>C |
| AA Mutation | p.Lys989Thr(p.K989T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11098595:11098595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2617T>G |
| AA Mutation | p.Leu873Val(p.L873V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11364840:11364840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1228T>G |
| AA Mutation | p.Leu410Val(p.L410V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11384697:11384697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376760091 |
| CDS Mutation | c.1145C>T |
| AA Mutation | p.Thr382Met(p.T382M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11384751:11384751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1091G>A |
| AA Mutation | p.Arg364His(p.R364H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11082719:11082719(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2765A>G |
| AA Mutation | p.Asp922Gly(p.D922G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11364842:11364842(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1226A>G |
| AA Mutation | p.Glu409Gly(p.E409G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 10992575:10992575(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3187C>T |
| AA Mutation | p.Arg1063Cys(p.R1063C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11384773:11384773(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1069G>A |
| AA Mutation | p.Ala357Thr(p.A357T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 10973556:10973556(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3575A>C |
| AA Mutation | p.Lys1192Thr(p.K1192T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11384874:11384874(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373393242 |
| CDS Mutation | c.968C>T |
| AA Mutation | p.Ser323Leu(p.S323L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11564959:11564959(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs550568397 |
| CDS Mutation | c.272G>A |
| AA Mutation | p.Ser91Asn(p.S91N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11384844:11384844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.998C>T |
| AA Mutation | p.Ser333Leu(p.S333L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11364837:11364837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1231C>T |
| AA Mutation | p.Arg411Trp(p.R411W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11082779:11082779(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs748058547 |
| CDS Mutation | c.2705G>A |
| AA Mutation | p.Arg902Gln(p.R902Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11384778:11384778(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1064C>T |
| AA Mutation | p.Thr355Met(p.T355M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11384836:11384836(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1006A>C |
| AA Mutation | p.Thr336Pro(p.T336P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11411645:11411645(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.330A>C |
| AA Mutation | p.Gln110His(p.Q110H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11732171:11732171(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.139A>G |
| AA Mutation | p.Thr47Ala(p.T47A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11346523:11346523(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760066114 |
| CDS Mutation | c.1477G>A |
| AA Mutation | p.Ala493Thr(p.A493T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11346377:11346377(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1623T>A |
| AA Mutation | p.Asp541Glu(p.D541E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 10992595:10992595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774846850 |
| CDS Mutation | c.3167C>T |
| AA Mutation | p.Thr1056Met(p.T1056M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11384725:11384725(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1117A>G |
| AA Mutation | p.Ser373Gly(p.S373G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11022824:11022824(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760214222 |
| CDS Mutation | c.2944C>T |
| AA Mutation | p.Arg982Trp(p.R982W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11364731:11364731(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1337C>T |
| AA Mutation | p.Pro446Leu(p.P446L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11346457:11346457(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1543C>T |
| AA Mutation | p.Pro515Ser(p.P515S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11732176:11732176(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.134C>T |
| AA Mutation | p.Thr45Ile(p.T45I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11199588:11199588(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1835C>T |
| AA Mutation | p.Ala612Val(p.A612V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11199513:11199513(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1910G>T |
| AA Mutation | p.Gly637Val(p.G637V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000304623 |
| Start | 11364740:11364740(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1328A>G |
| AA Mutation | p.Asp443Gly(p.D443G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11346509:11346509(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1491C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11364840:11364840(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1228T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11117477:11117477(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs778573833 |
| CDS Mutation | c.2250G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11159734:11159734(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs149766664 |
| CDS Mutation | c.2001C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11384783:11384783(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746777283 |
| CDS Mutation | c.1059C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11411590:11411590(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.385A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11098595:11098595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs775420264 |
| CDS Mutation | c.2617T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 10973630:10973630(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3501C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11022900:11022900(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374086847 |
| CDS Mutation | c.2868G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000304623 |
| Start | 11236793:11236793(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372124459 |
| CDS Mutation | c.1659G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |