Identification of novel variants of <i>XPA</i> and <i>POLH/XPV</i> genes in xeroderma pigmentosum patients in Vietnam

Xeroderma pigmentosum (XP) disorder is recognized as a genetic condition inherited by autosomal recessive fashion. XP results from a defective DNA repair mechanism that significantly increases skin cancer risk. Fifteen Vietnamese patients were investigated with typical clinical manifestations of XP. Eight XP genes (<i>XPA</i> to <i>XPG</i> and <i>POLH</i>/<i>XPV</i>) were sequenced using peripheral blood samples. Overall, three novel variants on the <i>XPA</i> and <i>XPV</i> genes were detected in members of two families. One novel missense variant c.388A>G (p.R130G) of <i>XPA</i> was found in three patients with XP group A, two novel variants: c.680G>A (p.C227Y) and c.1652dupC (p.Gln553Profs*8) of <i>XPV</i> in one patient with XP group F/G. Our study contributes to the recognition of new mutations in XP patients which have not been reported in Human Gene Mutation Database (HGMD).