| Variant #0000624111 (NC_000019.9:g.8654445G>A, NM_030957.2:c.1925C>T (ADAMTS10))
        
          | Chromosome | 19 |  
          | 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.8654445G>A |  
          | DNA change (hg38) | g.8589561G>A |  
          | Published as | ADAMTS10(NM_001282352.1):c.386C>T (p.(Thr129Met)), ADAMTS10(NM_030957.3):c.1925C>T (p.T642M) |  
          | ISCN | - |  
          | DB-ID | ADAMTS10_000048 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) | 0.00019 View details |  
          | Owner | VKGL-NL_Rotterdam |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Rotterdam |  
          | Date created | 2019-12-06 12:43:26 +01:00 (CET) |  
          | Date last edited | 2023-11-27 17:27:23 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
 |