Gene >> HMGB3
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000325307 |
| Start |
150986169:150986169(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.269C>A |
| AA Mutation |
p.Pro90His(p.P90H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000325307 |
| Start |
150987817:150987817(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.506C>T |
| AA Mutation |
p.Ala169Val(p.A169V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |