Primary Site >> Esophagus Cancer
Gene >> NFATC2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396009 |
| Start | 51523529:51523529(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.712G>A |
| AA Mutation | p.Val238Met(p.V238M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396009 |
| Start | 51523394:51523394(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs774669305 |
| CDS Mutation | c.847G>A |
| AA Mutation | p.Val283Met(p.V283M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000396009 |
| Start | 51432366:51432366(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs779382116 |
| CDS Mutation | c.2423C>T |
| AA Mutation | p.Ser808Leu(p.S808L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396009 |
| Start | 51523632:51523632(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs765804863 |
| CDS Mutation | c.609G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000396009 |
| Start | 51432644:51432644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs758351007 |
| CDS Mutation | c.2145C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000396009 |
| Start | 51523926:51523927(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.314_315insT |
| AA Mutation | p.Ala106GlyfsTer66(p.A106Gfs*66) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |