List of variants in gene RECQL4 reported as benign for not specified

Minimum submission review status:		Collection method:
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: 43

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HGVS	dbSNP	gnomAD frequency
NM_004260.4(RECQL4):c.3127T>C (p.Leu1043=)	rs4925828	0.98841
NM_004260.4(RECQL4):c.274T>C (p.Ser92Pro)	rs2721190	0.98532
NM_004260.4(RECQL4):c.801G>C (p.Glu267Asp)	rs4244612	0.41942
NM_004260.4(RECQL4):c.3236+13C>T	rs4244610	0.41215
NM_004260.4(RECQL4):c.1258+18G>A	rs4251689	0.38613
NM_004260.4(RECQL4):c.3393+8C>T	rs756627	0.37589
NM_004260.4(RECQL4):c.1621-15C>T	rs4244611	0.37577
NM_004260.4(RECQL4):c.3014G>A (p.Arg1005Gln)	rs4251691	0.36660
NM_004260.4(RECQL4):c.738C>T (p.Ser246=)	rs4244613	0.36043
NM_004260.4(RECQL4):c.1772C>T (p.Pro591Leu)	rs2721191	0.02663
NM_004260.4(RECQL4):c.1258+6A>T	rs34437789	0.02229
NM_004260.4(RECQL4):c.1565G>A (p.Arg522His)	rs35842750	0.02097
NM_004260.4(RECQL4):c.3393+9A>G	rs4251692	0.02095
NM_004260.4(RECQL4):c.2395G>A (p.Val799Met)	rs34293591	0.01793
NM_004260.4(RECQL4):c.2238G>A (p.Ala746=)	rs35215952	0.01004
NM_004260.4(RECQL4):c.1879-15C>A	rs35126141	0.00929
NM_004260.4(RECQL4):c.2636C>A (p.Pro879His)	rs137975310	0.00913
NM_004260.4(RECQL4):c.1564C>T (p.Arg522Cys)	rs35407712	0.00877
NM_004260.4(RECQL4):c.275C>T (p.Ser92Phe)	rs200516441	0.00876
NM_004260.4(RECQL4):c.2415C>T (p.Ala805=)	rs34735741	0.00600
NM_004260.4(RECQL4):c.309G>A (p.Pro103=)	rs4251688	0.00564
NM_004260.4(RECQL4):c.1395G>A (p.Thr465=)	rs34948955	0.00557
NM_004260.4(RECQL4):c.195C>G (p.Leu65=)	rs369163654	0.00449
NM_004260.4(RECQL4):c.1090G>A (p.Val364Met)	rs144637135	0.00427
NM_004260.4(RECQL4):c.3133G>A (p.Ala1045Thr)	rs35348691	0.00390
NM_004260.4(RECQL4):c.3314G>A (p.Gly1105Asp)	rs36078464	0.00371
NM_004260.4(RECQL4):c.543G>A (p.Gln181=)	rs34159914	0.00353
NM_004260.4(RECQL4):c.3337G>C (p.Gly1113Arg)	rs35101495	0.00313
NM_004260.4(RECQL4):c.2377C>T (p.Pro793Ser)	rs35098923	0.00307
NM_004260.4(RECQL4):c.3058G>A (p.Val1020Met)	rs114149451	0.00287
NM_004260.4(RECQL4):c.1954G>A (p.Val652Met)	rs61754061	0.00285
NM_004260.4(RECQL4):c.3392G>A (p.Arg1131Lys)	rs201369291	0.00274
NM_004260.4(RECQL4):c.3435G>C (p.Gln1145His)	rs61755066	0.00261
NM_004260.4(RECQL4):c.2463+6C>T	rs35029361	0.00229
NM_004260.4(RECQL4):c.891C>T (p.Asp297=)	rs34700133	0.00227
NM_004260.4(RECQL4):c.565G>A (p.Gly189Ser)	rs34371341	0.00204
NM_004260.4(RECQL4):c.615C>G (p.Pro205=)	rs35639991	0.00159
NM_004260.4(RECQL4):c.755C>T (p.Pro252Leu)	rs199773279	0.00005
NM_004260.4(RECQL4):c.212A>G (p.Glu71Gly)	rs34642881
NM_004260.4(RECQL4):c.2463+18_2463+19del	rs71320828
NM_004260.4(RECQL4):c.2557TGCACC[2] (p.853CT[2])	rs548804317
NM_004260.4(RECQL4):c.2601C>G (p.Ala867=)	rs34358597
NM_004260.4(RECQL4):c.465C>G (p.Val155=)	rs116137512

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