ClinVar for Gene (Select 10489) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3312500	NM_003579.4(RAD54L):c.1907G>A (p.Ser636Asn)	LRRC41, RAD54L (S636N +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312496	NM_003579.4(RAD54L):c.2005G>A (p.Glu669Lys)	LRRC41, RAD54L (E489K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312495	NM_003579.4(RAD54L):c.2145C>G (p.Leu715=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3312489	NM_003579.4(RAD54L):c.1896C>T (p.Phe632=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3312488	NM_003579.4(RAD54L):c.2152G>A (p.Glu718Lys)	LRRC41, RAD54L (E538K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312482	NM_003579.4(RAD54L):c.2084A>C (p.Asp695Ala)	LRRC41, RAD54L (D695A +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312478	NM_003579.4(RAD54L):c.2192T>C (p.Ile731Thr)	LRRC41, RAD54L (I551T +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312476	NM_003579.4(RAD54L):c.1953T>C (p.Asp651=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3312469	NM_003579.4(RAD54L):c.1899G>C (p.Gln633His)	LRRC41, RAD54L (Q633H +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312468	NM_003579.4(RAD54L):c.1917G>T (p.Lys639Asn)	LRRC41, RAD54L (K459N +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312460	NM_003579.4(RAD54L):c.1891A>C (p.Ile631Leu)	LRRC41, RAD54L (I631L +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312459	NM_003579.4(RAD54L):c.2040C>G (p.His680Gln)	LRRC41, RAD54L (H680Q +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312458	NM_003579.4(RAD54L):c.1925G>A (p.Ser642Asn)	LRRC41, RAD54L (S462N +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312433	NM_003579.4(RAD54L):c.2049T>C (p.Arg683=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3312431	NM_003579.4(RAD54L):c.1986G>A (p.Lys662=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3312426	NM_003579.4(RAD54L):c.2070C>T (p.Ile690=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3312425	NM_003579.4(RAD54L):c.2143C>A (p.Leu715Ile)	LRRC41, RAD54L (L535I +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3312423	NM_003579.4(RAD54L):c.2141G>A (p.Gly714Glu)	LRRC41, RAD54L (G714E +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3291643	NM_006369.5(LRRC41):c.1222G>A (p.Ala408Thr)	LRRC41 (A408T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291642	NM_006369.5(LRRC41):c.214A>G (p.Ile72Val)	LRRC41 (I72V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291641	NM_006369.5(LRRC41):c.1342C>G (p.Leu448Val)	LRRC41 (L448V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291640	NM_006369.5(LRRC41):c.1949G>A (p.Ser650Asn)	LRRC41 (S650N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223433	NM_003579.4(RAD54L):c.2243G>A (p.Ter748=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 3223432	NM_003579.4(RAD54L):c.2203T>G (p.Phe735Val)	LRRC41, RAD54L (F555V +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3223431	NM_003579.4(RAD54L):c.2183C>T (p.Ser728Phe)	LRRC41, RAD54L (S548F +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3223430	NM_003579.4(RAD54L):c.2168C>T (p.Ala723Val)	LRRC41, RAD54L (A543V +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3223429	NM_003579.4(RAD54L):c.2144T>G (p.Leu715Arg)	LRRC41, RAD54L (L535R +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3223428	NM_003579.4(RAD54L):c.2132A>T (p.Asp711Val)	LRRC41, RAD54L (D531V +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
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 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 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 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 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 3120705	NM_006369.5(LRRC41):c.973C>T (p.Arg325Trp)	LRRC41 (R325W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120704	NM_006369.5(LRRC41):c.872G>A (p.Arg291Gln)	LRRC41 (R291Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120703	NM_006369.5(LRRC41):c.790C>T (p.Arg264Cys)	LRRC41 (R264C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120701	NM_006369.5(LRRC41):c.521A>G (p.Gln174Arg)	LRRC41 (Q174R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120700	NM_006369.5(LRRC41):c.2434A>G (p.Met812Val)	LRRC41 (M812V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120699	NM_006369.5(LRRC41):c.2031C>A (p.Phe677Leu)	LRRC41 (F677L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120698	NM_006369.5(LRRC41):c.1915C>G (p.Leu639Val)	LRRC41 (L639V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120697	NM_006369.5(LRRC41):c.123C>A (p.Asn41Lys)	LRRC41 (N41K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120696	NM_006369.5(LRRC41):c.1139G>T (p.Ser380Ile)	LRRC41 (S380I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120695	NM_006369.5(LRRC41):c.1033C>A (p.Pro345Thr)	LRRC41 (P345T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2672311	Single allele	ARTN, ATP6V0B +1226 more	Inversion	Bilateral polymicrogyria	GLikely pathogenic
Select item 2638797	NM_003579.4(RAD54L):c.2213G>A (p.Arg738His)	LRRC41, RAD54L (R558H +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GLikely benign
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 2625173	NM_003579.4(RAD54L):c.2162A>G (p.Gln721Arg)	LRRC41, RAD54L (Q721R +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 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 2625161	NM_003579.4(RAD54L):c.2233G>T (p.Gly745Cys)	LRRC41, RAD54L (G745C +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 2619357	NM_006369.5(LRRC41):c.1636G>A (p.Ala546Thr)	LRRC41 (A546T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2618425	NM_006369.5(LRRC41):c.52G>T (p.Ala18Ser)	LRRC41 (A18S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615036	NM_006369.5(LRRC41):c.1546G>A (p.Gly516Ser)	LRRC41 (G516S)	Single nucleotide variant (missense variant)	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 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 2595064	NM_003579.4(RAD54L):c.2142G>A (p.Gly714=)	LRRC41, RAD54L	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2591226	NM_006369.5(LRRC41):c.1255A>T (p.Ile419Phe)	LRRC41 (I419F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589906	NM_006369.5(LRRC41):c.1634G>A (p.Arg545Gln)	LRRC41 (R545Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2585329	NM_003579.4(RAD54L):c.2209C>T (p.Gln737Ter)	LRRC41, RAD54L (Q737* +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 2562810	NM_003579.4(RAD54L):c.2229G>A (p.Gln743=)	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 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 2562792	NM_003579.4(RAD54L):c.2091T>C (p.Ser697=)	LRRC41, RAD54L	Single nucleotide variant (synonymous 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 2562784	NM_003579.4(RAD54L):c.2164G>A (p.Ala722Thr)	LRRC41, RAD54L (A542T +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 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 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 2560364	NM_003579.4(RAD54L):c.2142G>C (p.Gly714=)	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 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 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 2560352	NM_003579.4(RAD54L):c.2231G>A (p.Arg744Gln)	LRRC41, RAD54L (R564Q +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2550802	NM_006369.5(LRRC41):c.664A>G (p.Ile222Val)	LRRC41 (I222V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547165	NM_006369.5(LRRC41):c.941C>T (p.Pro314Leu)	LRRC41 (P314L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515645	NM_006369.5(LRRC41):c.115G>T (p.Gly39Cys)	LRRC41 (G39C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511504	NM_006369.5(LRRC41):c.1202G>A (p.Arg401His)	LRRC41 (R401H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508983	NM_006369.5(LRRC41):c.1213G>T (p.Gly405Trp)	LRRC41 (G405W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496816	NM_003579.4(RAD54L):c.2204T>C (p.Phe735Ser)	LRRC41, RAD54L (F555S +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 2496809	NM_003579.4(RAD54L):c.2182T>C (p.Ser728Pro)	LRRC41, RAD54L (S548P +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2493222	NM_006369.5(LRRC41):c.1000G>C (p.Gly334Arg)	LRRC41 (G334R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489897	NM_006369.5(LRRC41):c.781C>T (p.Pro261Ser)	LRRC41 (P261S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489588	NM_006369.5(LRRC41):c.1111A>G (p.Thr371Ala)	LRRC41 (T371A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480586	NM_006369.5(LRRC41):c.1177C>G (p.Arg393Gly)	LRRC41 (R393G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478062	NM_006369.5(LRRC41):c.29G>C (p.Arg10Pro)	LRRC41 (R10P)	Single nucleotide variant (missense variant)	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 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 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 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 2463353	NM_003579.4(RAD54L):c.2129C>G (p.Thr710Ser)	LRRC41, RAD54L (T530S +1 more)	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 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 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 2461681	NM_006369.5(LRRC41):c.962G>A (p.Arg321Gln)	LRRC41 (R321Q)	Single nucleotide variant (missense variant)	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 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 2447792	NM_003579.4(RAD54L):c.2217T>C (p.Ser739=)	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

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