ClinVar Miner

List of variants in gene BARD1 reported as likely benign for Hereditary breast ovarian cancer syndrome

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_000465.4(BARD1):c.215+59_215+60del rs67240037 0.01582
NM_000465.4(BARD1):c.1314+29C>G rs71579845 0.01508
NM_000465.4(BARD1):c.1972C>T (p.Arg658Cys) rs3738888 0.00736
NM_000465.4(BARD1):c.1678-60T>C rs4986842 0.00718
NM_000465.4(BARD1):c.159-42A>C rs148092589 0.00654
NM_000465.4(BARD1):c.1904-67A>G rs4986840 0.00623
NM_000465.4(BARD1):c.90T>A (p.Gly30=) rs150354152 0.00088
NM_000465.4(BARD1):c.842C>T (p.Pro281Leu) rs367890377 0.00021
NM_000465.4(BARD1):c.1127C>T (p.Ser376Leu) rs587782333 0.00009
NM_000465.4(BARD1):c.764A>G (p.Asn255Ser) rs138904906 0.00009
NM_000465.4(BARD1):c.1409A>G (p.Asn470Ser) rs587781976 0.00008
NM_000465.4(BARD1):c.2291T>C (p.Ile764Thr) rs587780030 0.00004
NM_000465.4(BARD1):c.773T>C (p.Ile258Thr) rs146223579 0.00004
NM_000465.4(BARD1):c.1533G>A (p.Lys511=) rs371785856 0.00003
NM_000465.4(BARD1):c.977A>G (p.Asn326Ser) rs779960429 0.00002
NM_000465.4(BARD1):c.1396-22del rs750290706 0.00001
NM_000465.4(BARD1):c.585T>C (p.Ala195=) rs876658532 0.00001
NM_000465.4(BARD1):c.735A>G (p.Gln245=) rs763378916 0.00001
NM_000465.4(BARD1):c.1080T>C (p.Pro360=) rs2106108809
NM_000465.4(BARD1):c.1162A>C (p.Ile388Leu) rs1553622215
NM_000465.4(BARD1):c.1569-87T>G rs2106039402
NM_000465.4(BARD1):c.159-65T>C rs113582954
NM_000465.4(BARD1):c.177G>A (p.Glu59=)
NM_000465.4(BARD1):c.1944A>G (p.Glu648=)
NM_000465.4(BARD1):c.2100C>T (p.Gly700=) rs1692220418
NM_000465.4(BARD1):c.222T>C (p.Cys74=) rs1168791343

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