Primary Site >> Stomach Cancer
Gene >> KCND1
| ID | 1 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000218176 |
| Start | 48962805:48962805(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1720C>T |
| AA Mutation | p.Arg574Cys(p.R574C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218176 |
| Start | 48969419:48969419(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.853G>A |
| AA Mutation | p.Asp285Asn(p.D285N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218176 |
| Start | 48969596:48969596(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs375813023 |
| CDS Mutation | c.676C>T |
| AA Mutation | p.Arg226Cys(p.R226C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218176 |
| Start | 48969722:48969722(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.550G>A |
| AA Mutation | p.Ala184Thr(p.A184T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218176 |
| Start | 48969967:48969967(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs147541534 |
| CDS Mutation | c.305G>A |
| AA Mutation | p.Arg102Gln(p.R102Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218176 |
| Start | 48969733:48969733(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.539A>G |
| AA Mutation | p.His180Arg(p.H180R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000218176 |
| Start | 48969751:48969751(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.521G>A |
| AA Mutation | p.Arg174Gln(p.R174Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000218176 |
| Start | 48969612:48969612(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.660G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000218176 |
| Start | 48969639:48969639(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782214056 |
| CDS Mutation | c.633C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000218176 |
| Start | 48969879:48969879(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.393C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000218176 |
| Start | 48969669:48969669(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs184160237 |
| CDS Mutation | c.603C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |