ClinVar Miner

List of variants reported as likely pathogenic for Breast-ovarian cancer, familial, susceptibility to, 4 by Myriad Genetics, Inc.

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Total variants: 48
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.576+1G>A rs781161543 0.00002
NM_002878.4(RAD51D):c.620C>T (p.Ser207Leu) rs370228071 0.00002
NM_002878.4(RAD51D):c.739-1G>A rs1555567202 0.00001
NM_002878.4(RAD51D):c.131_144+24del rs1064795716
NM_002878.4(RAD51D):c.144+1G>T rs2142477107
NM_002878.4(RAD51D):c.144+1dup
NM_002878.4(RAD51D):c.145-1G>A
NM_002878.4(RAD51D):c.145-2A>G rs2142474941
NM_002878.4(RAD51D):c.263+1G>A rs1555570242
NM_002878.4(RAD51D):c.264-1G>A rs2091622013
NM_002878.4(RAD51D):c.264-1G>T rs2091622013
NM_002878.4(RAD51D):c.264-2A>C rs1555568514
NM_002878.4(RAD51D):c.264-2A>G rs1555568514
NM_002878.4(RAD51D):c.345+2T>C rs876659394
NM_002878.4(RAD51D):c.345G>A (p.Gln115=) rs1555568469
NM_002878.4(RAD51D):c.345G>C (p.Gln115His) rs1555568469
NM_002878.4(RAD51D):c.346-1G>C rs1555568386
NM_002878.4(RAD51D):c.480+1G>T rs1597862471
NM_002878.4(RAD51D):c.481-1G>T
NM_002878.4(RAD51D):c.481-2A>G rs2091605461
NM_002878.4(RAD51D):c.576+1G>T rs781161543
NM_002878.4(RAD51D):c.577-2A>G rs1555567649
NM_002878.4(RAD51D):c.623dup (p.Thr209fs) rs1555567610
NM_002878.4(RAD51D):c.641dup (p.Leu215fs) rs1409088398
NM_002878.4(RAD51D):c.661_662del (p.Arg221fs)
NM_002878.4(RAD51D):c.667+1G>A
NM_002878.4(RAD51D):c.667+1G>T rs1597858666
NM_002878.4(RAD51D):c.667+2T>C
NM_002878.4(RAD51D):c.668-1G>A rs2142418872
NM_002878.4(RAD51D):c.668-2A>C rs1567726325
NM_002878.4(RAD51D):c.668-4_670delinsCC
NM_002878.4(RAD51D):c.694_697dup (p.Glu233fs) rs2142418516
NM_002878.4(RAD51D):c.694dup (p.Arg232fs)
NM_002878.4(RAD51D):c.738+1G>A rs1567726124
NM_002878.4(RAD51D):c.738+1G>T
NM_002878.4(RAD51D):c.752del (p.Ile251fs) rs1597856236
NM_002878.4(RAD51D):c.763_764del (p.Arg255fs)
NM_002878.4(RAD51D):c.766del (p.Asp256fs) rs1597856162
NM_002878.4(RAD51D):c.772_778del (p.Gly258fs) rs1064795045
NM_002878.4(RAD51D):c.774dup (p.Arg259fs) rs1555567170
NM_002878.4(RAD51D):c.787_791del (p.Ala263fs)
NM_002878.4(RAD51D):c.816dup (p.Ser273fs)
NM_002878.4(RAD51D):c.82+1G>A rs786202788
NM_002878.4(RAD51D):c.82+1G>C
NM_002878.4(RAD51D):c.82G>C (p.Val28Leu)
NM_002878.4(RAD51D):c.861dup (p.Gly288fs)
NM_002878.4(RAD51D):c.886del (p.Ala296fs) rs761589376
NM_002878.4(RAD51D):c.898del (p.Arg300fs) rs786202251

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