ClinVar Miner

List of variants in gene RAD51 reported as likely benign for not provided

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Gene type:
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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_002875.5(RAD51):c.531-303C>T rs114347852 0.01533
NM_002875.5(RAD51):c.531-48T>G rs45510195 0.01531
NM_002875.5(RAD51):c.896+271C>T rs45595939 0.01530
NM_002875.5(RAD51):c.87+290G>A rs8031306 0.01001
NM_002875.5(RAD51):c.225+314C>T rs45623631 0.00739
NM_002875.5(RAD51):c.225+426G>T rs45574037 0.00567
NM_002875.5(RAD51):c.164C>T (p.Ala55Val) rs145617142 0.00051
NM_002875.5(RAD51):c.720C>G (p.Ala240=) rs188331342 0.00027
NM_002875.5(RAD51):c.144T>C (p.Thr48=) rs140524566 0.00024
NM_002875.5(RAD51):c.945C>T (p.Tyr315=) rs139810756 0.00022
NM_002875.5(RAD51):c.1011C>T (p.Ala337=) rs202116013 0.00013
NM_002875.5(RAD51):c.531-12C>T rs752351863 0.00009
NM_002875.5(RAD51):c.696C>T (p.Tyr232=) rs766705075 0.00007
NM_002875.5(RAD51):c.402C>T (p.Thr134=) rs774860635 0.00001
NM_002875.5(RAD51):c.436-4A>G rs56391422 0.00001
NM_002875.5(RAD51):c.675C>T (p.Thr225=) rs147352002 0.00001
NM_002875.5(RAD51):c.1008T>C (p.Asp336=)
NM_002875.5(RAD51):c.108C>T (p.Asn36=)
NM_002875.5(RAD51):c.165G>T (p.Ala55=)
NM_002875.5(RAD51):c.225+190dup rs57054958
NM_002875.5(RAD51):c.225+600_225+601del rs35383252
NM_002875.5(RAD51):c.225+668C>T
NM_002875.5(RAD51):c.225+685T>C
NM_002875.5(RAD51):c.249A>G (p.Pro83=)
NM_002875.5(RAD51):c.258C>T (p.Phe86=)
NM_002875.5(RAD51):c.264T>C (p.Thr88=)
NM_002875.5(RAD51):c.279C>T (p.His93=)
NM_002875.5(RAD51):c.312T>C (p.Thr104=)
NM_002875.5(RAD51):c.324G>A (p.Glu108=)
NM_002875.5(RAD51):c.343+8A>C
NM_002875.5(RAD51):c.344-12T>C
NM_002875.5(RAD51):c.344-5T>A
NM_002875.5(RAD51):c.357T>G (p.Thr119=)
NM_002875.5(RAD51):c.378T>C (p.Phe126=)
NM_002875.5(RAD51):c.408C>A (p.Ile136=)
NM_002875.5(RAD51):c.414T>C (p.His138=)
NM_002875.5(RAD51):c.416C>T (p.Thr139Met)
NM_002875.5(RAD51):c.423T>C (p.Ala141=)
NM_002875.5(RAD51):c.426C>A (p.Val142=)
NM_002875.5(RAD51):c.429C>T (p.Thr143=)
NM_002875.5(RAD51):c.435+13G>T
NM_002875.5(RAD51):c.436-18T>C
NM_002875.5(RAD51):c.436-20G>T
NM_002875.5(RAD51):c.436-5T>C
NM_002875.5(RAD51):c.456A>T (p.Gly152=)
NM_002875.5(RAD51):c.468G>A (p.Lys156=)
NM_002875.5(RAD51):c.504A>G (p.Pro168=)
NM_002875.5(RAD51):c.530+172dup rs938761449
NM_002875.5(RAD51):c.530+8A>T rs1596008042
NM_002875.5(RAD51):c.531-12C>A
NM_002875.5(RAD51):c.531-14C>T
NM_002875.5(RAD51):c.564T>C (p.Asn188=)
NM_002875.5(RAD51):c.567A>G (p.Val189=) rs1407380775
NM_002875.5(RAD51):c.582G>A (p.Ala194=)
NM_002875.5(RAD51):c.600G>A (p.Gln200=)
NM_002875.5(RAD51):c.621A>T (p.Ala207=)
NM_002875.5(RAD51):c.645-11G>A
NM_002875.5(RAD51):c.645-17A>G
NM_002875.5(RAD51):c.671C>G (p.Ala224Gly)
NM_002875.5(RAD51):c.678C>G (p.Ala226=)
NM_002875.5(RAD51):c.699G>A (p.Ser233=) rs754954656
NM_002875.5(RAD51):c.760C>A (p.Arg254=)
NM_002875.5(RAD51):c.831G>A (p.Ala277=)
NM_002875.5(RAD51):c.87+17T>C
NM_002875.5(RAD51):c.879C>A (p.Ala293=)
NM_002875.5(RAD51):c.885A>G (p.Ala295=) rs779197451
NM_002875.5(RAD51):c.896+17A>T
NM_002875.5(RAD51):c.896+20A>T
NM_002875.5(RAD51):c.904C>T (p.Leu302=)
NM_002875.5(RAD51):c.927C>A (p.Thr309=)
NM_002875.5(RAD51):c.984C>A (p.Ala328=)

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