ClinVar for MedGen (Select 924579) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2500738	NM_002875.5(RAD51):c.340C>G (p.Gln114Glu)	RAD51 (Q114E)	Single nucleotide variant (missense variant +1 more)	Fanconi anemia complementation group R	GUncertain significance
Select item 2500726	NM_002875.5(RAD51):c.590C>T (p.Thr197Ile)	RAD51 (T197I +1 more)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group R	GLikely pathogenic
Select item 2443994	NM_002875.5(RAD51):c.871ATC[1] (p.Ile292del)	RAD51 (I292del +1 more)	Microsatellite (inframe_deletion +1 more)	Fanconi anemia complementation group R	GLikely pathogenic
Select item 916731	NM_002875.5(RAD51):c.391A>C (p.Thr131Pro)	RAD51 (T131P +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GPathogenic
Select item 522859	NM_002875.5(RAD51):c.772G>A (p.Glu258Lys)	RAD51 (E258K +1 more)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group R	GLikely pathogenic
Select item 372139	NM_002875.5(RAD51):c.877G>A (p.Ala293Thr)	RAD51 (A293T +1 more)	Single nucleotide variant (missense variant +1 more)	RAD51-related disorder +1 more	GPathogenic/Likely pathogenic

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