ÎÚÑ»´«Ã½

Jump to Main Content

Variant Information

Gene Interpretation
BCOR chrX:39923059 chrX:40063806 c.3547C>T p.R1183* Pathogenic
BCOR chrX:39921528 chrX:40062275 c.4190C>A p.S1397Y VUS
BCOR chrX:39914723 chrX:40055470 c.4537C>T p.R1513* Pathogenic
BCOR chrX:39911649 chrX:40052396 c.4879C>T p.R1627* Pathogenic