List of variants in gene combination RAD51D, RAD51L3-RFFL reported as pathogenic for cancer

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 21

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HGVS	dbSNP	gnomAD frequency
NM_002878.4(RAD51D):c.694C>T (p.Arg232Ter)	rs587780104	0.00004
NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter)	rs387906843	0.00003
NM_002878.4(RAD51D):c.898C>T (p.Arg300Ter)	rs750621215	0.00002
NM_002878.4(RAD51D):c.263+1503C>T	rs753486358	0.00001
NM_002878.4(RAD51D):c.739-1G>A	rs1555567202	0.00001
NM_002878.4(RAD51D):c.144+1dup
NM_002878.4(RAD51D):c.1A>G (p.Met1Val)	rs561425038
NM_002878.4(RAD51D):c.263+1617C>T
NM_002878.4(RAD51D):c.270_271dup (p.Lys91fs)	rs753862052
NM_002878.4(RAD51D):c.357_360del (p.Cys119fs)	rs876658297
NM_002878.4(RAD51D):c.480+1G>A	rs1597862471
NM_002878.4(RAD51D):c.574C>T (p.Gln192Ter)	rs2091602962
NM_002878.4(RAD51D):c.574del (p.Gln192fs)
NM_002878.4(RAD51D):c.738+402_*1465del
NM_002878.4(RAD51D):c.746del (p.Asn249fs)	rs2091536198
NM_002878.4(RAD51D):c.757C>T (p.Arg253Ter)	rs137886232
NM_002878.4(RAD51D):c.790_796dup (p.Arg266fs)	rs2142411968
NM_002878.4(RAD51D):c.866del (p.Gly289fs)
NM_002878.4(RAD51D):c.904-2A>T	rs1403784434
NM_002878.4(RAD51D):c.941G>A (p.Trp314Ter)
NM_002878.4(RAD51D):c.974del (p.Gly325fs)

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