NM_005807.6:c.923_924del

HGVS Expressions

  • NG_008248.2:g.15357_15358del
  • NM_005807.6:c.923_924del
  • NP_005798.3:p.Lys308fs

Associated Genes

Proteoglycan 4
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Genomic Location

chr1:186306642-186306643

Variant Type

Deletion

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
208250.2Saudi Arabia2Camptodactyly-Arthropathy-Coxa Vara-Pericarditis SyndromeAlazami et al. 2006 Patient 2 in the publication
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