ClinVar for Gene (Select 8438) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3362666	NM_003579.4(RAD54L):c.267T>G (p.Tyr89Ter)	RAD54L (Y89*)	Single nucleotide variant (nonsense +1 more)	Lymphoma, non-Hodgkin, familial	GLikely pathogenic
Select item 3312501	NM_003579.4(RAD54L):c.1123C>G (p.Gln375Glu)	RAD54L (Q195E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 3312499	NM_003579.4(RAD54L):c.547G>C (p.Asp183His)	RAD54L (D183H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312498	NM_003579.4(RAD54L):c.1770G>C (p.Met590Ile)	RAD54L (M410I +1 more)	Single nucleotide variant (missense variant)	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 3312494	NM_003579.4(RAD54L):c.874C>G (p.Leu292Val)	RAD54L (L112V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312493	NM_003579.4(RAD54L):c.1154C>A (p.Thr385Asn)	RAD54L (T205N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312492	NM_003579.4(RAD54L):c.335C>G (p.Pro112Arg)	RAD54L (P112R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312491	NM_003579.4(RAD54L):c.625C>G (p.Pro209Ala)	RAD54L (P209A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312490	NM_003579.4(RAD54L):c.1779T>G (p.Pro593=)	RAD54L	Single nucleotide variant (synonymous variant)	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 3312487	NM_003579.4(RAD54L):c.924T>C (p.Thr308=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3312485	NM_003579.4(RAD54L):c.1282C>G (p.Leu428Val)	RAD54L (L248V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312484	NM_003579.4(RAD54L):c.1123C>A (p.Gln375Lys)	RAD54L (Q375K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3312483	NM_003579.4(RAD54L):c.1462A>G (p.Lys488Glu)	RAD54L (K308E +1 more)	Single nucleotide variant (missense variant)	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 3312481	NM_003579.4(RAD54L):c.143T>G (p.Leu48Arg)	RAD54L (L48R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312480	NM_003579.4(RAD54L):c.969C>A (p.Ile323=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3312479	NM_003579.4(RAD54L):c.1435G>A (p.Asp479Asn)	RAD54L (D299N +1 more)	Single nucleotide variant (missense variant)	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 3312477	NM_003579.4(RAD54L):c.392A>C (p.Gln131Pro)	RAD54L (Q131P)	Single nucleotide variant (missense 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 3312474	NM_003579.4(RAD54L):c.187C>G (p.Pro63Ala)	RAD54L (P63A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312473	NM_003579.4(RAD54L):c.228C>G (p.Ser76Arg)	RAD54L (S76R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312472	NM_003579.4(RAD54L):c.829A>C (p.Thr277Pro)	RAD54L (T277P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312471	NM_003579.4(RAD54L):c.1665T>C (p.Val555=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3312470	NM_003579.4(RAD54L):c.1464G>C (p.Lys488Asn)	RAD54L (K488N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 3312467	NM_003579.4(RAD54L):c.139T>G (p.Phe47Val)	RAD54L (F47V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312466	NM_003579.4(RAD54L):c.1143G>T (p.Leu381=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3312465	NM_003579.4(RAD54L):c.1579G>T (p.Asp527Tyr)	RAD54L (D347Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312463	NM_003579.4(RAD54L):c.718C>G (p.Pro240Ala)	RAD54L (P60A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312462	NM_003579.4(RAD54L):c.453G>C (p.Lys151Asn)	RAD54L (K151N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312461	NM_003579.4(RAD54L):c.1423G>T (p.Val475Leu)	RAD54L (V475L +1 more)	Single nucleotide variant (missense variant)	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 3312457	NM_003579.4(RAD54L):c.371C>T (p.Pro124Leu)	RAD54L (P124L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312456	NM_003579.4(RAD54L):c.311G>T (p.Gly104Val)	RAD54L (G104V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312455	NM_003579.4(RAD54L):c.712A>G (p.Ile238Val)	RAD54L (I238V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312454	NM_003579.4(RAD54L):c.146C>A (p.Ser49Tyr)	RAD54L (S49Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312452	NM_003579.4(RAD54L):c.979C>A (p.Pro327Thr)	RAD54L (P147T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312451	NM_003579.4(RAD54L):c.988A>G (p.Asn330Asp)	RAD54L (N150D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312450	NM_003579.4(RAD54L):c.1434G>C (p.Leu478Phe)	RAD54L (L478F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312449	NM_003579.4(RAD54L):c.1692C>G (p.Ser564Arg)	RAD54L (S384R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312448	NM_003579.4(RAD54L):c.1071T>G (p.Phe357Leu)	RAD54L (F357L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312447	NM_003579.4(RAD54L):c.733G>A (p.Gly245Arg)	RAD54L (G245R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312446	NM_003579.4(RAD54L):c.1596G>C (p.Leu532=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3312445	NM_003579.4(RAD54L):c.470A>G (p.Gln157Arg)	RAD54L (Q157R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312444	NM_003579.4(RAD54L):c.678G>T (p.Trp226Cys)	RAD54L (W226C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312443	NM_003579.4(RAD54L):c.825T>C (p.Tyr275=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3312440	NM_003579.4(RAD54L):c.814A>C (p.Ile272Leu)	RAD54L (I272L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312439	NM_003579.4(RAD54L):c.815T>C (p.Ile272Thr)	RAD54L (I92T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312438	NM_003579.4(RAD54L):c.20C>T (p.Pro7Leu)	RAD54L (P7L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312437	NM_003579.4(RAD54L):c.1364A>C (p.Lys455Thr)	RAD54L (K275T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312436	NM_003579.4(RAD54L):c.1319G>A (p.Gly440Asp)	RAD54L (G440D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312434	NM_003579.4(RAD54L):c.1013T>C (p.Leu338Ser)	RAD54L (L158S +1 more)	Single nucleotide variant (missense variant)	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 3312432	NM_003579.4(RAD54L):c.1274A>T (p.Lys425Met)	RAD54L (K425M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 3312430	NM_003579.4(RAD54L):c.1357C>T (p.Leu453=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3312429	NM_003579.4(RAD54L):c.733G>C (p.Gly245Arg)	RAD54L (G65R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312427	NM_003579.4(RAD54L):c.255C>T (p.Pro85=)	RAD54L	Single nucleotide variant (synonymous 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 3312422	NM_003579.4(RAD54L):c.694A>G (p.Lys232Glu)	RAD54L (K232E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312421	NM_003579.4(RAD54L):c.1657G>C (p.Ala553Pro)	RAD54L (A553P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312420	NM_003579.4(RAD54L):c.353T>C (p.Leu118Ser)	RAD54L (L118S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312418	NM_003579.4(RAD54L):c.1470G>A (p.Leu490=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3312417	NM_003579.4(RAD54L):c.209A>G (p.His70Arg)	RAD54L (H70R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223475	NM_003579.4(RAD54L):c.997C>T (p.Leu333Phe)	RAD54L (L153F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223474	NM_003579.4(RAD54L):c.98G>A (p.Arg33Lys)	RAD54L (R33K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3223473	NM_003579.4(RAD54L):c.935T>A (p.Leu312Gln)	RAD54L (L132Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223471	NM_003579.4(RAD54L):c.919C>G (p.Gln307Glu)	RAD54L (Q127E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223469	NM_003579.4(RAD54L):c.900G>A (p.Arg300=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3223468	NM_003579.4(RAD54L):c.8G>A (p.Arg3Lys)	RAD54L (R3K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223467	NM_003579.4(RAD54L):c.872G>A (p.Gly291Asp)	RAD54L (G111D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223466	NM_003579.4(RAD54L):c.871G>T (p.Gly291Cys)	RAD54L (G111C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223465	NM_003579.4(RAD54L):c.830C>T (p.Thr277Ile)	RAD54L (T277I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223463	NM_003579.4(RAD54L):c.803C>A (p.Ser268Tyr)	RAD54L (S268Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223462	NM_003579.4(RAD54L):c.776T>A (p.Met259Lys)	RAD54L (M259K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223461	NM_003579.4(RAD54L):c.768A>G (p.Glu256=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3223460	NM_003579.4(RAD54L):c.756C>A (p.Asp252Glu)	RAD54L (D252E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223459	NM_003579.4(RAD54L):c.754G>A (p.Asp252Asn)	RAD54L (D252N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223458	NM_003579.4(RAD54L):c.725C>T (p.Ala242Val)	RAD54L (A242V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223457	NM_003579.4(RAD54L):c.724G>A (p.Ala242Thr)	RAD54L (A242T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223456	NM_003579.4(RAD54L):c.696A>G (p.Lys232=)	RAD54L	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3223455	NM_003579.4(RAD54L):c.688G>A (p.Val230Ile)	RAD54L (V230I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223453	NM_003579.4(RAD54L):c.646G>A (p.Val216Met)	RAD54L (V216M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3223451	NM_003579.4(RAD54L):c.542T>C (p.Met181Thr)	RAD54L (M181T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223450	NM_003579.4(RAD54L):c.541A>C (p.Met181Leu)	RAD54L (M181L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223449	NM_003579.4(RAD54L):c.509G>A (p.Ser170Asn)	RAD54L (S170N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223448	NM_003579.4(RAD54L):c.508A>G (p.Ser170Gly)	RAD54L (S170G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223447	NM_003579.4(RAD54L):c.502G>A (p.Val168Ile)	RAD54L (V168I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3223446	NM_003579.4(RAD54L):c.464C>T (p.Pro155Leu)	RAD54L (P155L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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