List of variants in gene RAD51 studied for Fanconi anemia complementation group R

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_002875.5(RAD51):c.340C>G (p.Gln114Glu)
NM_002875.5(RAD51):c.391A>C (p.Thr131Pro)	rs1895530875
NM_002875.5(RAD51):c.590C>T (p.Thr197Ile)
NM_002875.5(RAD51):c.772G>A (p.Glu258Lys)	rs1555429629
NM_002875.5(RAD51):c.871ATC[1] (p.Ile292del)
NM_002875.5(RAD51):c.877G>A (p.Ala293Thr)	rs1057519413

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