| Variant #0000016591 (NC_000015.9:g.40710430_40710459del, NM_002225.3:c.(1249_1278del) (IVD))
        
          | Chromosome | 15 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Affects function |  
          | Affects function (by curator) | Probably affects function |  
          | Classification method | - |  
          | Clinical classification | NA |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.40710430_40710459del |  
          | DNA change (hg38) | g.40418231_40418260del |  
          | Published as | DEL10 |  
          | ISCN | - |  
          | DB-ID | IVD_000017 |  
          | Variant remarks | No IVD activity found |  
          | Reference | PubMed: Volchenboum et al (2000) |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | In vitro (cloned) |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Ivo F.A.C. Fokkema |  
          | Database submission license | Creative Commons Attribution-ShareAlike 4.0 International   |  
          | Created by | Ivo F.A.C. Fokkema |  
          | Date created | 2012-11-27 23:02:44 +01:00 (CET) |  
          | Date last edited | 2020-07-14 21:50:58 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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