Primary Site >> Stomach Cancer
Gene >> NKD1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268459 |
| Start | 50633425:50633425(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1057G>A |
| AA Mutation | p.Gly353Ser(p.G353S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268459 |
| Start | 50633602:50633602(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1234G>T |
| AA Mutation | p.Gly412Cys(p.G412C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268459 |
| Start | 50549470:50549470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.107A>T |
| AA Mutation | p.Glu36Val(p.E36V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268459 |
| Start | 50633347:50633347(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.979A>G |
| AA Mutation | p.Lys327Glu(p.K327E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268459 |
| Start | 50633375:50633375(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757531250 |
| CDS Mutation | c.1007G>A |
| AA Mutation | p.Arg336Gln(p.R336Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268459 |
| Start | 50633255:50633255(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs751057016 |
| CDS Mutation | c.887G>A |
| AA Mutation | p.Arg296His(p.R296H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268459 |
| Start | 50608330:50608330(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs369647847 |
| CDS Mutation | c.229G>A |
| AA Mutation | p.Glu77Lys(p.E77K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000268459 |
| Start | 50625504:50625504(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.386C>T |
| AA Mutation | p.Ser129Phe(p.S129F) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268459 |
| Start | 50633250:50633250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs760115281 |
| CDS Mutation | c.882A>G |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268459 |
| Start | 50608305:50608305(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.204C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000268459 |
| Start | 50625496:50625496(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372034222 |
| CDS Mutation | c.378C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | inframe_deletion |
| Transcription ID | ENST00000268459 |
| Start | 50549458:50549469(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.97_108delGGCATCGAGGAG |
| AA Mutation | p.Gly33_Glu36del(p.G33_E36del) |
| Mutation Classification | In_Frame_Del |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | inframe_insertion |
| Transcription ID | ENST00000268459 |
| Start | 50549469:50549470(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.114_115insAAGTGGATC |
| AA Mutation | p.Ile38_Gly39insLysTrpIle(p.I38_G39insKWI) |
| Mutation Classification | In_Frame_Ins |
| Feature Type | Transcript |