| Variant #0000001502 (NC_000017.10:g.57141716C>T, NM_015294.3:c.860G>A (TRIM37))
        
          | Chromosome | 17 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Affects function |  
          | Classification method | - |  
          | Clinical classification | pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.57141716C>T |  
          | DNA change (hg38) | g.59064355C>T |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | TRIM37_000006 |  
          | Variant remarks | 1 Australian MUL patient (com-het) |  
          | Reference | PubMed: Hämäläinen et al. 2006 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | yes |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Anne Polvi |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Anne Polvi |  
          | Date created | 2012-08-29 12:00:21 +02:00 (CEST) |  
          | Date last edited | 2017-05-05 19:04:32 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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