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    | Variant #0000538846 (NC_000010.10:g.101483828G>A, NM_078470.4:c.635C>T (COX15))
        
          | 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.101483828G>A |  
          | DNA change (hg38) | g.99724071G>A |  
          | Published as | COX15(NM_004376.5):c.635C>T (p.(Ser212Phe)), COX15(NM_078470.4):c.635C>T (p.S212F) |  
          | ISCN | - |  
          | DB-ID | COX15_000005 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) | Retrieve |  
          | Owner | VKGL-NL_Rotterdam |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Rotterdam |  
          | Date created | 2019-07-18 18:22:55 +02:00 (CEST) |  
          | Date last edited | 2019-12-04 15:24:38 +01:00 (CET) |   
 
 
 
       
 
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