| Variant #0000617959 (NC_000019.9:g.8649945_8649951dup, NC_000019.9(NM_030957.2):c.3043-12_3043-6dup (ADAMTS10))
        
          | Chromosome | 19 |  
          | Allele | Unknown |  
          | Affects function (as reported) | Probably does not affect function |  
          | Affects function (by curator) | Not classified |  
          | Classification method | - |  
          | Clinical classification | likely benign |  
          | DNA change (genomic) (Relative to hg19 / GRCh37) | g.8649945_8649951dup |  
          | DNA change (hg38) | g.8585061_8585067dup |  
          | Published as | ADAMTS10(NM_030957.2):c.3043-6_3043-5insGCCCCCT (p.?), ADAMTS10(NM_030957.4):c.3043-6_3043-5insGCCCCCT |  
          | ISCN | - |  
          | DB-ID | ADAMTS10_000011 See all 3 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_Leiden |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | VKGL-NL_Leiden |  
          | Date created | 2019-12-04 15:24:38 +01:00 (CET) |  
          | Date last edited | 2023-01-11 15:44:22 +01:00 (CET) |   
 
 
 
       
 
 Variant on transcripts
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