Primary Site >> Stomach Cancer
Gene >> CARD14
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344227 |
| Start | 80189820:80189820(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.911G>A |
| AA Mutation | p.Arg304His(p.R304H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344227 |
| Start | 80182700:80182700(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs370897817 |
| CDS Mutation | c.259G>A |
| AA Mutation | p.Ala87Thr(p.A87T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344227 |
| Start | 80207037:80207037(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2759C>A |
| AA Mutation | p.Pro920His(p.P920H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344227 |
| Start | 80188411:80188411(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.710A>G |
| AA Mutation | p.Asn237Ser(p.N237S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344227 |
| Start | 80184107:80184107(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372403419 |
| CDS Mutation | c.544C>T |
| AA Mutation | p.Arg182Cys(p.R182C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344227 |
| Start | 80207025:80207025(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2747T>C |
| AA Mutation | p.Met916Thr(p.M916T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344227 |
| Start | 80208250:80208250(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs767247623 |
| CDS Mutation | c.2920G>T |
| AA Mutation | p.Gly974Cys(p.G974C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000344227 |
| Start | 80202320:80202320(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs757622443 |
| CDS Mutation | c.2119G>A |
| AA Mutation | p.Asp707Asn(p.D707N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344227 |
| Start | 80198465:80198465(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.1729delG |
| AA Mutation | p.Asp577MetfsTer40(p.D577Mfs*40) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000344227 |
| Start | 80202226:80202226(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs758713305 |
| CDS Mutation | c.2029delG |
| AA Mutation | p.Asp677ThrfsTer45(p.D677Tfs*45) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |