Variant #0000921836 (NC_000016.9:g.67199717C>T, NM_001374675.1:c.328C>T (HSF4))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.67199717C>T |
| DNA change (hg38) |
g.67165814C>T |
| Published as |
R120C |
| ISCN |
- |
| DB-ID |
HSF4_000019 See all 2 reported entries |
| Variant remarks |
markedly inhibited HSF4b oligomerization, inhibits transcription activation ability of HSF4b due to defective HSE-binding |
| Reference |
PubMed: Enoki 2010 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2023-03-21 19:18:05 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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