| Variant #0000539197 (NC_000010.10:g.115338424C>T, NM_004132.3:c.607C>T (HABP2))
        
          | Chromosome | 10 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | VUS |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.115338424C>T |  
          | DNA change (hg38) | g.113578665C>T |  
          | Published as | HABP2(NM_001177660.1):c.529C>T (p.(Arg177*)), HABP2(NM_004132.4):c.607C>T (p.R203*), HABP2(NM_004132.5):c.607C>T (p.R203*) |  
          | ISCN | - |  
          | DB-ID | HABP2_000006 See all 3 reported entries |  
          | Variant remarks | VKGL data sharing initiative Nederland |  
          | Reference | - |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | CLASSIFICATION record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | 0.00203 View details |  
          | Owner | VKGL-NL_Leiden |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Leiden |  
          | Date created | 2019-07-18 18:22:55 +02:00 (CEST) |  
          | Date last edited | 2023-04-16 21:50:28 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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