| Variant #0000433565 (NC_000003.11:g.37035142T>G, NM_000249.3:c.104T>G (MLH1))
        
          | Chromosome | 3 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Effect unknown |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | NA |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.37035142T>G |  
          | DNA change (hg38) | g.36993651T>G |  
          | Published as | M35R |  
          | ISCN | - |  
          | DB-ID | MLH1_000952 See all 29 reported entries |  
          | Variant remarks | {GR:50} |  
          | Reference | PubMed: Kondo 2003 |  
          | ClinVar ID | - |  
          | dbSNP ID | - |  
          | Origin | In vitro (cloned) |  
          | Segregation | - |  
          | Frequency | - |  
          | Re-site | - |  
          | VIP | - |  
          | Methylation | - |  
          | Average frequency (gnomAD v.2.1.1) | Retrieve |  
          | Owner | Rolf Sijmons |  
          | Database submission license | No license selected |  
          | Created by | Rolf Sijmons |  
          | Date created | 2009-02-06 12:00:00 +01:00 (CET) |  
          | Date last edited | 2019-02-20 13:06:39 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
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