Primary Site >> Stomach Cancer
Gene >> DIO3
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000510508 |
| Start | 101561726:101561726(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.230G>A |
| AA Mutation | p.Arg77Gln(p.R77Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000510508 |
| Start | 101561975:101561975(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.479C>T |
| AA Mutation | p.Pro160Leu(p.P160L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000510508 |
| Start | 101561851:101561851(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.355C>T |
| AA Mutation | p.His119Tyr(p.H119Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000510508 |
| Start | 101561961:101561961(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs540396975 |
| CDS Mutation | c.465G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000510508 |
| Start | 101561886:101561886(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs367842454 |
| CDS Mutation | c.390C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000510508 |
| Start | 101562387:101562387(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.891C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000510508 |
| Start | 101561883:101561883(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs376085567 |
| CDS Mutation | c.387G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |