ClinVar Miner

List of variants in gene SLX4 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_032444.4(SLX4):c.90C>T (p.Ser30=) rs118089506 0.00612
NM_032444.4(SLX4):c.5501A>G (p.Asn1834Ser) rs111738042 0.00575
NM_032444.4(SLX4):c.4648C>T (p.Arg1550Trp) rs77021998 0.00214
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.590T>C (p.Val197Ala) rs147826749 0.00115
NM_032444.4(SLX4):c.4479G>A (p.Ser1493=) rs150097733 0.00112
NM_032444.4(SLX4):c.3774C>T (p.Pro1258=) rs146054214 0.00085
NM_032444.4(SLX4):c.339T>C (p.Ser113=) rs144326379 0.00061
NM_032444.4(SLX4):c.3178C>T (p.Arg1060Trp) rs144273492 0.00059
NM_032444.4(SLX4):c.4836C>T (p.Asp1612=) rs140844106 0.00051
NM_032444.4(SLX4):c.3189C>T (p.Gly1063=) rs200742809 0.00047
NM_032444.4(SLX4):c.4494G>A (p.Leu1498=) rs146532299 0.00041
NM_032444.4(SLX4):c.231A>G (p.Gln77=) rs143279888 0.00038
NM_032444.4(SLX4):c.1470C>T (p.Leu490=) rs139766312 0.00031
NM_032444.4(SLX4):c.3663G>A (p.Ala1221=) rs760656992 0.00029
NM_032444.4(SLX4):c.1065G>A (p.Gln355=) rs200183071 0.00022
NM_032444.4(SLX4):c.465A>G (p.Glu155=) rs138512851 0.00020
NM_032444.4(SLX4):c.1809G>A (p.Ser603=) rs565202250 0.00017
NM_032444.4(SLX4):c.832C>T (p.Arg278Trp) rs141597706 0.00014
NM_032444.4(SLX4):c.2235C>T (p.Thr745=) rs75184268 0.00012
NM_032444.4(SLX4):c.833G>A (p.Arg278Gln) rs201192909 0.00011
NM_032444.4(SLX4):c.2006G>A (p.Arg669His) rs200807331 0.00009
NM_032444.4(SLX4):c.192A>G (p.Lys64=) rs756720856 0.00007
NM_032444.4(SLX4):c.4149C>T (p.Phe1383=) rs983816841 0.00007
NM_032444.4(SLX4):c.165C>T (p.Cys55=) rs202030834 0.00006
NM_032444.4(SLX4):c.2100G>A (p.Gly700=) rs755000337 0.00005
NM_032444.4(SLX4):c.246C>T (p.Asn82=) rs1021522087 0.00004
NM_032444.4(SLX4):c.2490G>A (p.Ala830=) rs753595071 0.00004
NM_032444.4(SLX4):c.3873G>A (p.Thr1291=) rs751302297 0.00004
NM_032444.4(SLX4):c.4456A>C (p.Arg1486=) rs200536796 0.00004
NM_032444.4(SLX4):c.570T>G (p.Pro190=) rs764067884 0.00004
NM_032444.4(SLX4):c.3471G>A (p.Ser1157=) rs748090102 0.00002
NM_032444.4(SLX4):c.846G>A (p.Ser282=) rs745750001 0.00002
NM_032444.4(SLX4):c.1251G>A (p.Pro417=) rs780972710 0.00001
NM_032444.4(SLX4):c.2925G>A (p.Pro975=) rs1431725463 0.00001
NM_032444.4(SLX4):c.3153A>G (p.Thr1051=) rs1484366381 0.00001
NM_032444.4(SLX4):c.3634G>A (p.Ala1212Thr) rs574844562 0.00001
NM_032444.4(SLX4):c.3912C>T (p.Val1304=) rs140254478 0.00001
NM_032444.4(SLX4):c.4056G>A (p.Pro1352=) rs768415277 0.00001
NM_032444.4(SLX4):c.4098C>T (p.Arg1366=) rs770811758 0.00001
NM_032444.4(SLX4):c.4824A>G (p.Ser1608=) rs767845523 0.00001
NM_032444.4(SLX4):c.1014T>C (p.Ile338=)
NM_032444.4(SLX4):c.1254C>G (p.Ser418=)
NM_032444.4(SLX4):c.1395G>A (p.Pro465=) rs569518866
NM_032444.4(SLX4):c.1407A>C (p.Pro469=)
NM_032444.4(SLX4):c.1521G>A (p.Arg507=)
NM_032444.4(SLX4):c.1755C>A (p.Pro585=) rs114016359
NM_032444.4(SLX4):c.258AAG[1] (p.Arg87del) rs536289991
NM_032444.4(SLX4):c.2622C>T (p.Gly874=)
NM_032444.4(SLX4):c.3630C>T (p.Ser1210=) rs1567169951
NM_032444.4(SLX4):c.3876C>T (p.Pro1292=)
NM_032444.4(SLX4):c.421G>T (p.Gly141Trp) rs137976282
NM_032444.4(SLX4):c.4554G>A (p.Glu1518=)
NM_032444.4(SLX4):c.4617C>G (p.Pro1539=)
NM_032444.4(SLX4):c.5097T>C (p.Ser1699=) rs202099433
NM_032444.4(SLX4):c.60G>A (p.Leu20=) rs200430973

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