| Variant #0000619975 (NC_000023.10:g.99888952A>G, NM_003270.2:c.426T>C (TSPAN6))
        
          | Chromosome | X |  
          | 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.99888952A>G |  
          | DNA change (hg38) | g.100633955A>G |  
          | Published as | TSPAN6(NM_001278740.1):c.162T>C (p.H54=) |  
          | ISCN | - |  
          | DB-ID | TSPAN6_000007 |  
          | 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 | 2019-12-04 15:24:38 +01:00 (CET) |  
          | Date last edited | 2020-07-20 17:38:05 +02:00 (CEST) |   
 
 
 
       
 
 Variant on transcripts
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