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    | Variant #0000921832 (NC_000016.9:g.67200261G>C, NM_001374675.1:c.524G>C (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.67200261G>C |  
          | DNA change (hg38) | g.67166358G>C |  
          | Published as | R176P |  
          | ISCN | - |  
          | DB-ID | HSF4_000009 See all 3 reported entries |  
          | Variant remarks | 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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