ClinVar Miner

List of variants in gene SLX4 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 101
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HGVS dbSNP gnomAD frequency
NM_032444.4(SLX4):c.2824G>C (p.Glu942Gln) rs114014006 0.01879
NM_032444.4(SLX4):c.-104A>G rs73505426 0.01460
NM_032444.4(SLX4):c.761-32T>G rs118098382 0.01011
NM_032444.4(SLX4):c.1684-64C>T rs112856971 0.01008
NM_032444.4(SLX4):c.2160+23G>A rs116556108 0.01006
NM_032444.4(SLX4):c.1924+99C>T rs113684042 0.01004
NM_032444.4(SLX4):c.4338C>T (p.Thr1446=) rs77718962 0.00998
NM_032444.4(SLX4):c.5146T>A (p.Ser1716Thr) rs75182789 0.00995
NM_032444.4(SLX4):c.1164-111C>T rs114573935 0.00983
NM_032444.4(SLX4):c.760+151C>G rs60172682 0.00972
NM_032444.4(SLX4):c.1153C>A (p.Pro385Thr) rs115694169 0.00968
NM_032444.4(SLX4):c.2746G>T (p.Ala916Ser) rs79448721 0.00968
NM_032444.4(SLX4):c.2161-136G>A rs139226142 0.00967
NM_032444.4(SLX4):c.4115G>A (p.Arg1372Gln) rs79174372 0.00921
NM_032444.4(SLX4):c.710G>A (p.Arg237Gln) rs138615800 0.00848
NM_032444.4(SLX4):c.1898G>A (p.Gly633Asp) rs1056085 0.00810
NM_032444.4(SLX4):c.3963G>A (p.Pro1321=) rs116781836 0.00774
NM_032444.4(SLX4):c.1924+19C>A rs113075119 0.00694
NM_032444.4(SLX4):c.2924C>T (p.Pro975Leu) rs114472821 0.00679
NM_032444.4(SLX4):c.1803G>A (p.Ser601=) rs144892556 0.00649
NM_032444.4(SLX4):c.1925-30G>A rs149916101 0.00641
NM_032444.4(SLX4):c.1755C>T (p.Pro585=) rs114016359 0.00638
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.718A>G (p.Asn240Asp) rs114744903 0.00474
NM_032444.4(SLX4):c.4637-242G>A rs111410156 0.00453
NM_032444.4(SLX4):c.761-179G>A rs145323994 0.00448
NM_032444.4(SLX4):c.950+189C>T rs145710480 0.00448
NM_032444.4(SLX4):c.2160+45T>C rs192085750 0.00383
NM_032444.4(SLX4):c.5029C>T (p.Pro1677Ser) rs7196345 0.00363
NM_032444.4(SLX4):c.3857C>T (p.Ala1286Val) rs149011965 0.00302
NM_032444.4(SLX4):c.1924+127G>A rs563725168 0.00261
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.2305G>C (p.Glu769Gln) rs150712805 0.00119
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.1924+33C>T rs374393051 0.00081
NM_032444.4(SLX4):c.2786C>T (p.Pro929Leu) rs117707719 0.00078
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.4344C>T (p.Pro1448=) rs368388100 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.335C>T (p.Pro112Leu) rs1333549121 0.00003
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.4902C>T (p.Tyr1634=) rs749720194 0.00001
NM_032444.4(SLX4):c.1014T>C (p.Ile338=)
NM_032444.4(SLX4):c.1029T>C (p.Phe343=) rs1363185627
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.1896G>A (p.Gly632=) rs200859735
NM_032444.4(SLX4):c.2160+24C>A rs114392599
NM_032444.4(SLX4):c.2160+280A>C rs77679067
NM_032444.4(SLX4):c.2328-203G>A
NM_032444.4(SLX4):c.258AAG[1] (p.Arg87del) rs536289991
NM_032444.4(SLX4):c.2622C>T (p.Gly874=)
NM_032444.4(SLX4):c.3510C>T (p.Ser1170=) rs1384973981
NM_032444.4(SLX4):c.3621A>C (p.Pro1207=) rs1436426423
NM_032444.4(SLX4):c.3630C>T (p.Ser1210=) rs1567169951
NM_032444.4(SLX4):c.3876C>T (p.Pro1292=)
NM_032444.4(SLX4):c.3969A>T (p.Ser1323=) rs753327971
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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