| Variant #0000612712 (NC_000010.10:g.88441223G>A, NC_000010.10(NM_001080114.1):c.321+1309G>A (LDB3))
        
          | Chromosome | 10 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Does not affect function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.88441223G>A |  
          | DNA change (hg38) | g.86681466G>A |  
          | Published as | LDB3(NM_001080115.1):c.352G>A (p.(Val118Met)), LDB3(NM_001171610.2):c.352G>A (p.V118M), LDB3(NM_007078.2):c.352G>A (p.V118M) |  
          | ISCN | - |  
          | DB-ID | LDB3_000127 See all 6 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) | 0.0043 View details |  
          | Owner | VKGL-NL_Nijmegen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Nijmegen |  
          | Date created | 2019-12-04 15:24:38 +01:00 (CET) |  
          | Date last edited | 2023-04-16 21:50:28 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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