| Variant #0000903260 (NC_000017.10:g.57168657_57168660del, NC_000017.10(NM_015294.3):c.164+3_164+6del (TRIM37))
        
          | Chromosome | 17 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably affects function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | likely pathogenic |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.57168657_57168660del |  
          | DNA change (hg38) | - |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | TRIM37_000067 See all 2 reported entries |  
          | Variant remarks | - |  
          | Reference | - |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | Unknown |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | MobiDetails |  
          | Database submission license | Creative Commons Attribution 4.0 International   |  
          | Created by | MobiDetails |  
          | Date created | 2022-11-24 10:55:01 +01:00 (CET) |  
          | Date last edited | N/A |   
 
 
 
       
 
 Variant on transcripts
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