Primary Site >> Stomach Cancer
Gene >> DIO2
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438257 |
| Start | 80202841:80202841(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.670G>A |
| AA Mutation | p.Gly224Arg(p.G224R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438257 |
| Start | 80211286:80211286(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.187G>A |
| AA Mutation | p.Val63Ile(p.V63I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438257 |
| Start | 80211319:80211319(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.154C>T |
| AA Mutation | p.Arg52Trp(p.R52W) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000438257 |
| Start | 80202801:80202801(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.710A>C |
| AA Mutation | p.Lys237Thr(p.K237T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000438257 |
| Start | 80202884:80202884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.627A>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000438257 |
| Start | 80211417:80211417(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | rs148778534 |
| CDS Mutation | c.56delT |
| AA Mutation | p.Phe19SerfsTer23(p.F19Sfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000438257 |
| Start | 80203231:80203232(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.279dupA |
| AA Mutation | p.Gly94ArgfsTer3(p.G94Rfs*3) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |