Primary Site >> Stomach Cancer
Gene >> CDH3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68695868:68695868(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2225C>T |
| AA Mutation | p.Pro742Leu(p.P742L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68679927:68679927(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199812197 |
| CDS Mutation | c.820C>T |
| AA Mutation | p.Arg274Trp(p.R274W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000264012 |
| Start | 68695255:68695255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2003T>G |
| AA Mutation | p.Phe668Cys(p.F668C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68684591:68684591(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1191T>A |
| AA Mutation | p.Asp397Glu(p.D397E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68676451:68676451(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374865506 |
| CDS Mutation | c.227G>A |
| AA Mutation | p.Arg76Gln(p.R76Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68682416:68682416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374738611 |
| CDS Mutation | c.1111G>A |
| AA Mutation | p.Gly371Ser(p.G371S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68681032:68681032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs527796702 |
| CDS Mutation | c.932C>T |
| AA Mutation | p.Thr311Met(p.T311M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68678774:68678774(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.559G>A |
| AA Mutation | p.Ala187Thr(p.A187T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68678186:68678186(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757633932 |
| CDS Mutation | c.299G>A |
| AA Mutation | p.Arg100His(p.R100H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68682392:68682392(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs74026937 |
| CDS Mutation | c.1087C>T |
| AA Mutation | p.Arg363Cys(p.R363C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68685285:68685285(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1505A>G |
| AA Mutation | p.Asp502Gly(p.D502G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000264012 |
| Start | 68691828:68691828(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1904C>T |
| AA Mutation | p.Ala635Val(p.A635V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264012 |
| Start | 68678584:68678584(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs140049723 |
| CDS Mutation | c.474C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264012 |
| Start | 68698328:68698328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs749006688 |
| CDS Mutation | c.2418C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264012 |
| Start | 68684621:68684621(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368241091 |
| CDS Mutation | c.1221C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000264012 |
| Start | 68698394:68698394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs202210726 |
| CDS Mutation | c.2484C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |