"Ambry Genetics"[submitter] AND "LRRC41"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1781698	NM_003579.4(RAD54L):c.1871C>T (p.Ala624Val)	LRRC41, RAD54L (A444V +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1781765	NM_003579.4(RAD54L):c.1875G>C (p.Gly625=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1781777	NM_003579.4(RAD54L):c.1876A>G (p.Thr626Ala)	LRRC41, RAD54L (T446A +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1781797	NM_003579.4(RAD54L):c.1877C>T (p.Thr626Ile)	LRRC41, RAD54L (T446I +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1781816	NM_003579.4(RAD54L):c.1878C>G (p.Thr626=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2560355	NM_003579.4(RAD54L):c.1881T>C (p.Ile627=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1781972	NM_003579.4(RAD54L):c.1885G>A (p.Glu629Lys)	LRRC41, RAD54L (E449K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1782005	NM_003579.4(RAD54L):c.1888A>G (p.Lys630Glu)	LRRC41, RAD54L (K630E +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2625160	NM_003579.4(RAD54L):c.1889A>T (p.Lys630Met)	LRRC41, RAD54L (K630M +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1782073	NM_003579.4(RAD54L):c.1891A>G (p.Ile631Val)	LRRC41, RAD54L (I631V +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2561507	NM_003579.4(RAD54L):c.1892T>A (p.Ile631Asn)	LRRC41, RAD54L (I451N +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1782128	NM_003579.4(RAD54L):c.1894T>C (p.Phe632Leu)	LRRC41, RAD54L (F452L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2447810	NM_003579.4(RAD54L):c.1895T>G (p.Phe632Cys)	LRRC41, RAD54L (F632C +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2595426	NM_003579.4(RAD54L):c.1896C>A (p.Phe632Leu)	LRRC41, RAD54L (F452L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2465204	NM_003579.4(RAD54L):c.1901G>A (p.Arg634His)	LRRC41, RAD54L (R454H +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1782416	NM_003579.4(RAD54L):c.1907G>C (p.Ser636Thr)	LRRC41, RAD54L (S636T +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1782460	NM_003579.4(RAD54L):c.1909C>G (p.His637Asp)	LRRC41, RAD54L (H637D +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1782497	NM_003579.4(RAD54L):c.1910A>G (p.His637Arg)	LRRC41, RAD54L (H457R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1782496	NM_003579.4(RAD54L):c.1910A>C (p.His637Pro)	LRRC41, RAD54L (H637P +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1782558	NM_003579.4(RAD54L):c.1914G>A (p.Lys638=)	LRRC41, RAD54L	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3223421	NM_003579.4(RAD54L):c.1921C>T (p.Leu641=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1782728	NM_003579.4(RAD54L):c.1923G>A (p.Leu641=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2560356	NM_003579.4(RAD54L):c.1926C>T (p.Ser642=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1782785	NM_003579.4(RAD54L):c.1927A>G (p.Ser643Gly)	LRRC41, RAD54L (S463G +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2447817	NM_003579.4(RAD54L):c.1931G>A (p.Cys644Tyr)	LRRC41, RAD54L (C644Y +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1782920	NM_003579.4(RAD54L):c.1933G>A (p.Val645Met)	RAD54L, LRRC41 (V645M +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1782939	NM_003579.4(RAD54L):c.1934T>G (p.Val645Gly)	LRRC41, RAD54L (V465G +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2595875	NM_003579.4(RAD54L):c.1938G>A (p.Val646=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1782999	NM_003579.4(RAD54L):c.1938G>T (p.Val646=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1783066	NM_003579.4(RAD54L):c.1941T>C (p.Asp647=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1783061	NM_003579.4(RAD54L):c.1941T>A (p.Asp647Glu)	LRRC41, RAD54L (D467E +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2462989	NM_003579.4(RAD54L):c.1944G>C (p.Glu648Asp)	LRRC41, RAD54L (E648D +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1783101	NM_003579.4(RAD54L):c.1944G>A (p.Glu648=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2447788	NM_003579.4(RAD54L):c.1950G>C (p.Gln650His)	LRRC41, RAD54L (Q470H +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1783225	NM_003579.4(RAD54L):c.1950G>A (p.Gln650=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2562807	NM_003579.4(RAD54L):c.1951G>T (p.Asp651Tyr)	LRRC41, RAD54L (D651Y +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1783279	NM_003579.4(RAD54L):c.1954G>A (p.Val652Ile)	LRRC41, RAD54L (V472I +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2561513	NM_003579.4(RAD54L):c.1957G>A (p.Glu653Lys)	LRRC41, RAD54L (E473K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1783372	NM_003579.4(RAD54L):c.1959G>C (p.Glu653Asp)	LRRC41, RAD54L (E473D +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1783370	NM_003579.4(RAD54L):c.1959G>A (p.Glu653=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1783423	NM_003579.4(RAD54L):c.1960C>T (p.Arg654Cys)	LRRC41, RAD54L (R474C +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2561510	NM_003579.4(RAD54L):c.1963C>T (p.His655Tyr)	LRRC41, RAD54L (H655Y +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1783508	NM_003579.4(RAD54L):c.1965C>T (p.His655=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1783506	NM_003579.4(RAD54L):c.1965C>A (p.His655Gln)	LRRC41, RAD54L (H475Q +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1783572	NM_003579.4(RAD54L):c.1969T>A (p.Ser657Thr)	LRRC41, RAD54L (S477T +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1783610	NM_003579.4(RAD54L):c.1970C>G (p.Ser657Cys)	LRRC41, RAD54L (S477C +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1783664	NM_003579.4(RAD54L):c.1973T>C (p.Leu658Pro)	LRRC41, RAD54L (L478P +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3223423	NM_003579.4(RAD54L):c.1974G>C (p.Leu658=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1783676	NM_003579.4(RAD54L):c.1974G>A (p.Leu658=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1783749	NM_003579.4(RAD54L):c.1978G>A (p.Glu660Lys)	LRRC41, RAD54L (E660K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2562803	NM_003579.4(RAD54L):c.1980G>A (p.Glu660=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1783824	NM_003579.4(RAD54L):c.1981T>G (p.Leu661Val)	LRRC41, RAD54L (L661V +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1783846	NM_003579.4(RAD54L):c.1983G>A (p.Leu661=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1783909	NM_003579.4(RAD54L):c.1989G>A (p.Glu663=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1783990	NM_003579.4(RAD54L):c.1992G>A (p.Leu664=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1784046	NM_003579.4(RAD54L):c.1995T>C (p.Phe665=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1784051	NM_003579.4(RAD54L):c.1996A>G (p.Ile666Val)	LRRC41, RAD54L (I666V +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2625170	NM_003579.4(RAD54L):c.1998C>T (p.Ile666=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1784089	NM_003579.4(RAD54L):c.1998C>G (p.Ile666Met)	LRRC41, RAD54L (I486M +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1784302	NM_003579.4(RAD54L):c.2004T>A (p.Asp668Glu)	RAD54L, LRRC41 (D668E +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2625174	NM_003579.4(RAD54L):c.2010T>C (p.Ala670=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2625169	NM_003579.4(RAD54L):c.2014C>T (p.Leu672Phe)	LRRC41, RAD54L (L492F +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3223424	NM_003579.4(RAD54L):c.2017A>G (p.Ser673Gly)	LRRC41, RAD54L (S493G +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1784505	NM_003579.4(RAD54L):c.2019T>A (p.Ser673Arg)	LRRC41, RAD54L (S493R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1784585	NM_003579.4(RAD54L):c.2022C>T (p.Asp674=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1678937	NM_003579.4(RAD54L):c.2026C>T (p.His676Tyr)	LRRC41, RAD54L (H496Y +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1784663	NM_003579.4(RAD54L):c.2027A>G (p.His676Arg)	LRRC41, RAD54L (H496R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1784702	NM_003579.4(RAD54L):c.2028T>C (p.His676=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1784963	NM_003579.4(RAD54L):c.2046A>G (p.Arg682=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2463264	NM_003579.4(RAD54L):c.2047C>T (p.Arg683Cys)	LRRC41, RAD54L (R683C +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3223425	NM_003579.4(RAD54L):c.2048G>T (p.Arg683Leu)	LRRC41, RAD54L (R503L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1785074	NM_003579.4(RAD54L):c.2050T>C (p.Cys684Arg)	LRRC41, RAD54L (C684R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1785079	NM_003579.4(RAD54L):c.2051G>A (p.Cys684Tyr)	LRRC41, RAD54L (C504Y +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1785159	NM_003579.4(RAD54L):c.2058C>T (p.Asn686=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1785155	NM_003579.4(RAD54L):c.2058C>A (p.Asn686Lys)	RAD54L, LRRC41 (N686K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1785173	NM_003579.4(RAD54L):c.2059A>G (p.Ser687Gly)	LRRC41, RAD54L (S507G +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2496814	NM_003579.4(RAD54L):c.2061C>G (p.Ser687Arg)	LRRC41, RAD54L (S687R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1678940	NM_003579.4(RAD54L):c.2063G>A (p.Arg688His)	LRRC41, RAD54L (R508H +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary breast ovarian cancer syndrome +1 more	GLikely benign
Select item 3223426	NM_003579.4(RAD54L):c.2067G>C (p.Gln689His)	LRRC41, RAD54L (Q509H +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2463077	NM_003579.4(RAD54L):c.2072G>A (p.Arg691Gln)	LRRC41, RAD54L (R691Q +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1785441	NM_003579.4(RAD54L):c.2074C>T (p.Pro692Ser)	LRRC41, RAD54L (P692S +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1785452	NM_003579.4(RAD54L):c.2075C>T (p.Pro692Leu)	LRRC41, RAD54L (P512L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1785490	NM_003579.4(RAD54L):c.2078C>T (p.Pro693Leu)	LRRC41, RAD54L (P513L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2560353	NM_003579.4(RAD54L):c.2079C>T (p.Pro693=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2466449	NM_003579.4(RAD54L):c.2080C>A (p.Pro694Thr)	LRRC41, RAD54L (P514T +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2464347	NM_003579.4(RAD54L):c.2080C>T (p.Pro694Ser)	LRRC41, RAD54L (P514S +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1785555	NM_003579.4(RAD54L):c.2080C>G (p.Pro694Ala)	LRRC41, RAD54L (P514A +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2466625	NM_003579.4(RAD54L):c.2082T>C (p.Pro694=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2562792	NM_003579.4(RAD54L):c.2091T>C (p.Ser697=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1785913	NM_003579.4(RAD54L):c.2100T>C (p.Thr700=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2562791	NM_003579.4(RAD54L):c.2102C>T (p.Ser701Leu)	LRRC41, RAD54L (S521L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1785991	NM_003579.4(RAD54L):c.2106C>T (p.Asp702=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1786013	NM_003579.4(RAD54L):c.2108T>C (p.Leu703Pro)	LRRC41, RAD54L (L523P +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1786033	NM_003579.4(RAD54L):c.2109G>C (p.Leu703=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1786115	NM_003579.4(RAD54L):c.2111C>G (p.Ala704Gly)	LRRC41, RAD54L (A524G +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1786141	NM_003579.4(RAD54L):c.2113G>A (p.Gly705Arg)	LRRC41, RAD54L (G525R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1786247	NM_003579.4(RAD54L):c.2121C>T (p.Asn707=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1786288	NM_003579.4(RAD54L):c.2124C>T (p.His708=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 1786286	NM_003579.4(RAD54L):c.2124C>G (p.His708Gln)	LRRC41, RAD54L (H528Q +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 1786316	NM_003579.4(RAD54L):c.2125T>C (p.Cys709Arg)	LRRC41, RAD54L (C529R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance

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