Gene >> HMGB2
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000296503 |
| Start |
173332178:173332178(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.532C>T |
| AA Mutation |
p.Pro178Ser(p.P178S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000296503 |
| Start |
173333188:173333188(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.177G>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |