"Sema4, Sema4"[submitter] AND "LOC130061310"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 478777	NM_058216.3(RAD51C):c.145+5C>A	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O +1 more	GUncertain significance
Select item 138870	NM_058216.3(RAD51C):c.145+12T>G	LOC130061310, RAD51C	Single nucleotide variant (intron variant)	Fanconi anemia complementation group O +4 more	GConflicting classifications of pathogenicity