| Variant #0000540186 (NC_000010.10:g.64950833C>G, NM_004241.2:c.5401G>C (JMJD1C))
        
          | 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.64950833C>G |  
          | DNA change (hg38) | g.63191073C>G |  
          | Published as | JMJD1C(NM_032776.2):c.6112G>C (p.E2038Q), JMJD1C(NM_032776.3):c.6112G>C (p.E2038Q) |  
          | ISCN | - |  
          | DB-ID | JMJD1C_000007 See all 2 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) | 0.00041 View details |  
          | Owner | VKGL-NL_Groningen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Groningen |  
          | Date created | 2019-07-18 18:22:55 +02:00 (CEST) |  
          | Date last edited | 2023-01-11 15:44:22 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
 |