ClinVar Miner

List of variants in gene SLX4 reported as uncertain significance by GeneDx

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Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_032444.4(SLX4):c.2290C>G (p.Pro764Ala) rs151105762 0.00218
NM_032444.4(SLX4):c.2103G>C (p.Glu701Asp) rs73505420 0.00210
NM_032444.4(SLX4):c.422G>T (p.Gly141Val) rs77306735 0.00131
NM_032444.4(SLX4):c.2359G>A (p.Glu787Lys) rs140600202 0.00125
NM_032444.4(SLX4):c.2305G>C (p.Glu769Gln) rs150712805 0.00119
NM_032444.4(SLX4):c.3676C>T (p.Arg1226Trp) rs142008398 0.00114
NM_032444.4(SLX4):c.2047G>A (p.Ala683Thr) rs115866745 0.00092
NM_032444.4(SLX4):c.1372A>G (p.Lys458Glu) rs149126845 0.00087
NM_032444.4(SLX4):c.85C>T (p.Arg29Cys) rs144832924 0.00078
NM_032444.4(SLX4):c.2756C>T (p.Thr919Ile) rs145533919 0.00052
NM_032444.4(SLX4):c.2654C>T (p.Pro885Leu) rs147492092 0.00036
NM_032444.4(SLX4):c.2681T>G (p.Val894Gly) rs145137472 0.00036
NM_032444.4(SLX4):c.3671A>T (p.Glu1224Val) rs566584111 0.00036
NM_032444.4(SLX4):c.2210G>A (p.Arg737His) rs146901714 0.00029
NM_032444.4(SLX4):c.742G>A (p.Glu248Lys) rs148547201 0.00024
NM_032444.4(SLX4):c.1829A>G (p.Gln610Arg) rs544935776 0.00019
NM_032444.4(SLX4):c.3940C>A (p.Gln1314Lys) rs142040192 0.00016
NM_032444.4(SLX4):c.2437G>A (p.Glu813Lys) rs770020510 0.00011
NM_032444.4(SLX4):c.3068C>A (p.Ala1023Asp) rs769271628 0.00006
NM_032444.4(SLX4):c.5188T>C (p.Ser1730Pro) rs199838670 0.00006
NM_032444.4(SLX4):c.-602-6C>G rs886051986 0.00005
NM_032444.4(SLX4):c.1640C>T (p.Thr547Met) rs755156257 0.00005
NM_032444.4(SLX4):c.4046G>C (p.Gly1349Ala) rs151144102 0.00005
NM_032444.4(SLX4):c.3622C>G (p.Pro1208Ala) rs752941190 0.00004
NM_032444.4(SLX4):c.734C>T (p.Pro245Leu) rs199929086 0.00004
NM_032444.4(SLX4):c.1520G>A (p.Arg507Lys) rs762550449 0.00003
NM_032444.4(SLX4):c.3062G>C (p.Arg1021Pro) rs200842643 0.00003
NM_032444.4(SLX4):c.553G>A (p.Asp185Asn) rs201769293 0.00003
NM_032444.4(SLX4):c.1255G>A (p.Glu419Lys) rs941244697 0.00002
NM_032444.4(SLX4):c.217G>C (p.Glu73Gln) rs139829211 0.00002
NM_032444.4(SLX4):c.3962C>T (p.Pro1321Leu) rs778781581 0.00002
NM_032444.4(SLX4):c.5060C>G (p.Pro1687Arg) rs765960272 0.00002
NM_032444.4(SLX4):c.1162A>T (p.Ser388Cys) rs199774640 0.00001
NM_032444.4(SLX4):c.1841A>T (p.Asp614Val) rs966027727 0.00001
NM_032444.4(SLX4):c.2021T>G (p.Leu674Arg) rs889646690 0.00001
NM_032444.4(SLX4):c.2464A>G (p.Met822Val) rs779985555 0.00001
NM_032444.4(SLX4):c.2621G>A (p.Gly874Asp) rs150402424 0.00001
NM_032444.4(SLX4):c.3041G>A (p.Arg1014Lys) rs756448789 0.00001
NM_032444.4(SLX4):c.340G>A (p.Gly114Ser) rs764213293 0.00001
NM_032444.4(SLX4):c.4312A>G (p.Ile1438Val) rs746452357 0.00001
NM_032444.4(SLX4):c.4768C>G (p.Gln1590Glu) rs148228302 0.00001
NM_032444.4(SLX4):c.4927G>T (p.Ala1643Ser) rs145557355 0.00001
NM_032444.4(SLX4):c.5144G>A (p.Ser1715Asn) rs754498907 0.00001
NM_032444.4(SLX4):c.5384G>A (p.Arg1795His) rs926700658 0.00001
NM_032444.4(SLX4):c.1553A>G (p.Gln518Arg)
NM_032444.4(SLX4):c.1957A>C (p.Thr653Pro) rs2040643790
NM_032444.4(SLX4):c.2113G>A (p.Ala705Thr) rs749913190
NM_032444.4(SLX4):c.2371A>G (p.Ile791Val) rs1422973391
NM_032444.4(SLX4):c.2464A>T (p.Met822Leu) rs779985555
NM_032444.4(SLX4):c.258AAG[1] (p.Arg87del) rs536289991
NM_032444.4(SLX4):c.2675C>T (p.Ala892Val) rs1368217140
NM_032444.4(SLX4):c.4057C>A (p.His1353Asn) rs142205392
NM_032444.4(SLX4):c.421G>C (p.Gly141Arg) rs137976282
NM_032444.4(SLX4):c.421G>T (p.Gly141Trp) rs137976282
NM_032444.4(SLX4):c.4481_4525del (p.Gly1494_Ser1508del) rs750613465
NM_032444.4(SLX4):c.5150A>C (p.Gln1717Pro) rs766089444
NM_032444.4(SLX4):c.5231A>G (p.Gln1744Arg) rs2151115896
NM_032444.4(SLX4):c.760+5G>A rs1555452262

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