Primary Site >> Stomach Cancer
Gene >> CDH11
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64950866:64950866(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1795G>A |
| AA Mutation | p.Gly599Arg(p.G599R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64971995:64971995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1460A>C |
| AA Mutation | p.Lys487Thr(p.K487T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64998567:64998567(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.518A>C |
| AA Mutation | p.Asn173Thr(p.N173T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 65004704:65004704(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.166G>A |
| AA Mutation | p.Val56Ile(p.V56I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64982231:64982231(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1070A>C |
| AA Mutation | p.Lys357Thr(p.K357T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64950797:64950797(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1864G>A |
| AA Mutation | p.Ala622Thr(p.A622T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64982257:64982257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1044G>C |
| AA Mutation | p.Glu348Asp(p.E348D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64971641:64971641(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1580T>G |
| AA Mutation | p.Phe527Cys(p.F527C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64998660:64998660(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.425C>T |
| AA Mutation | p.Pro142Leu(p.P142L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64950839:64950839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1822G>A |
| AA Mutation | p.Ala608Thr(p.A608T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64948025:64948025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1969C>T |
| AA Mutation | p.Arg657Cys(p.R657C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64973026:64973026(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202032642 |
| CDS Mutation | c.1268G>A |
| AA Mutation | p.Arg423His(p.R423H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64948057:64948057(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1937A>G |
| AA Mutation | p.Glu646Gly(p.E646G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64971995:64971995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1460A>T |
| AA Mutation | p.Lys487Met(p.K487M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64991807:64991807(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.772C>A |
| AA Mutation | p.Leu258Met(p.L258M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64982122:64982122(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1179A>C |
| AA Mutation | p.Gln393His(p.Q393H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64971602:64971602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1619A>T |
| AA Mutation | p.Asn540Ile(p.N540I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64988197:64988197(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs373083222 |
| CDS Mutation | c.959C>T |
| AA Mutation | p.Thr320Met(p.T320M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64971995:64971995(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1460A>G |
| AA Mutation | p.Lys487Arg(p.K487R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64971603:64971603(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1618A>G |
| AA Mutation | p.Asn540Asp(p.N540D) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64982117:64982117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1184A>G |
| AA Mutation | p.Asn395Ser(p.N395S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64971600:64971600(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1621T>C |
| AA Mutation | p.Phe541Leu(p.F541L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64947662:64947662(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2332C>A |
| AA Mutation | p.Arg778Ser(p.R778S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64982238:64982238(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1063G>A |
| AA Mutation | p.Asp355Asn(p.D355N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 65004721:65004721(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.149G>A |
| AA Mutation | p.Arg50His(p.R50H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64982255:64982255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1046C>A |
| AA Mutation | p.Ala349Glu(p.A349E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64948094:64948094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1900G>T |
| AA Mutation | p.Val634Leu(p.V634L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64947917:64947917(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757580985 |
| CDS Mutation | c.2077C>T |
| AA Mutation | p.Arg693Cys(p.R693C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64998595:64998595(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.490T>A |
| AA Mutation | p.Tyr164Asn(p.Y164N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64948063:64948063(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1931A>C |
| AA Mutation | p.Lys644Thr(p.K644T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64992932:64992932(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs746370506 |
| CDS Mutation | c.626C>T |
| AA Mutation | p.Ser209Leu(p.S209L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64998711:64998711(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779652408 |
| CDS Mutation | c.374C>T |
| AA Mutation | p.Thr125Met(p.T125M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268603 |
| Start | 64973027:64973027(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1267C>G |
| AA Mutation | p.Arg423Gly(p.R423G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268603 |
| Start | 64947993:64947993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2001G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268603 |
| Start | 65004759:65004759(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.111G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268603 |
| Start | 64982071:64982071(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1230T>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268603 |
| Start | 64947858:64947858(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2136C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268603 |
| Start | 64947765:64947765(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs145843219 |
| CDS Mutation | c.2229C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000268603 |
| Start | 65004691:65004691(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.179delT |
| AA Mutation | p.Phe60SerfsTer3(p.F60Sfs*3) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000268603 |
| Start | 64992933:64992933(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.625delT |
| AA Mutation | p.Ser209ArgfsTer27(p.S209Rfs*27) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |