| Variant #0000355714 (NC_000003.11:g.37035147G>A, NM_000249.3:c.109G>A (MLH1))
        
          | Chromosome | 3 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Effect unknown |  
          | Classification method | InSiGHT |  
          | Clinical classification | VUS |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.37035147G>A |  
          | DNA change (hg38) | g.36993656G>A |  
          | Published as | - |  
          | ISCN | - |  
          | DB-ID | MLH1_000817 See all 5 reported entries |  
          | Variant remarks | Insight class: 3 |  
          | Reference | InSiGHT |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | SUMMARY record |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | InSiGHT - John-Paul Plazzer |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2018-03-05 12:40:48 +01:00 (CET) |  
          | Date last edited | 2020-06-12 15:43:14 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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