ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_032444.4(SLX4):c.4500T>C (p.Asn1500=) rs3810812 0.63612
NM_032444.4(SLX4):c.4636+194C>T rs8058233 0.42926
NM_032444.4(SLX4):c.1683+282C>T rs2240885 0.34039
NM_032444.4(SLX4):c.753G>A (p.Ala251=) rs8061528 0.21914
NM_032444.4(SLX4):c.3365C>T (p.Pro1122Leu) rs714181 0.20566
NM_032444.4(SLX4):c.-602-172T>C rs59127692 0.09493
NM_032444.4(SLX4):c.-359C>G rs57910835 0.09336
NM_032444.4(SLX4):c.536-335A>G rs78469607 0.09179
NM_032444.4(SLX4):c.4739+24G>T rs12933120 0.09148
NM_032444.4(SLX4):c.1366+11T>C rs76350200 0.08654
NM_032444.4(SLX4):c.*8A>G rs3751839 0.08334
NM_032444.4(SLX4):c.4740-146T>C rs758748 0.07977
NM_032444.4(SLX4):c.-602-228T>C rs60918224 0.07954
NM_032444.4(SLX4):c.-295A>G rs59311338 0.07951
NM_032444.4(SLX4):c.2854G>A (p.Ala952Thr) rs59939128 0.07918
NM_032444.4(SLX4):c.2012T>C (p.Leu671Ser) rs77985244 0.07388
NM_032444.4(SLX4):c.2013+137G>C rs80186343 0.07384
NM_032444.4(SLX4):c.610C>T (p.Arg204Cys) rs79842542 0.07023
NM_032444.4(SLX4):c.1371T>G (p.Asn457Lys) rs74319927 0.06397
NM_032444.4(SLX4):c.2013+183A>G rs112385346 0.06391
NM_032444.4(SLX4):c.1152A>G (p.Pro384=) rs112511042 0.06386
NM_032444.4(SLX4):c.761-298A>G rs79331723 0.06386
NM_032444.4(SLX4):c.1156A>G (p.Met386Val) rs113490934 0.06384
NM_032444.4(SLX4):c.951-79G>A rs111705152 0.06384
NM_032444.4(SLX4):c.2013+23G>A rs112226642 0.06373
NM_032444.4(SLX4):c.2160+50C>T rs75762935 0.06369
NM_032444.4(SLX4):c.950+172T>C rs74369366 0.05940
NM_032444.4(SLX4):c.4637-227C>T rs75693937 0.05798
NM_032444.4(SLX4):c.4637-318A>C rs74788216 0.05789
NM_032444.4(SLX4):c.*113C>T rs76661336 0.04982
NM_032444.4(SLX4):c.536-265G>A rs78956406 0.04964
NM_032444.4(SLX4):c.555C>T (p.Asp185=) rs74640850 0.04956
NM_032444.4(SLX4):c.535+210T>C rs80035526 0.04954
NM_032444.4(SLX4):c.2855C>T (p.Ala952Val) rs78637028 0.04932
NM_032444.4(SLX4):c.3662C>T (p.Ala1221Val) rs3827530 0.04930
NM_032444.4(SLX4):c.678C>T (p.His226=) rs28516461 0.04916
NM_032444.4(SLX4):c.3812C>T (p.Ser1271Phe) rs3810813 0.04718
NM_032444.4(SLX4):c.3162G>A (p.Ser1054=) rs76488917 0.03405
NM_032444.4(SLX4):c.1925-215C>G rs2240883 0.03399
NM_032444.4(SLX4):c.951-232C>T rs60163083 0.02934
NM_032444.4(SLX4):c.-602-26A>C rs78173617 0.02859
NM_032444.4(SLX4):c.4739+171T>C rs77425493 0.02321
NM_032444.4(SLX4):c.4739+198T>A rs75753413 0.02309
NM_032444.4(SLX4):c.3783G>A (p.Pro1261=) rs77699867 0.02290
NM_032444.4(SLX4):c.4581G>A (p.Pro1527=) rs78635099 0.02283
NM_032444.4(SLX4):c.4637-110T>C rs74005837 0.02262
NM_032444.4(SLX4):c.1683+118C>T rs113168577 0.02096
NM_032444.4(SLX4):c.2824G>C (p.Glu942Gln) rs114014006 0.01879
NM_032444.4(SLX4):c.3868C>A (p.His1290Asn) rs112596894 0.01345
NM_032444.4(SLX4):c.5281C>T (p.Arg1761Cys) rs143818824 0.00776
NM_032444.4(SLX4):c.1637A>G (p.Tyr546Cys) rs150547487 0.00416
NM_032444.4(SLX4):c.4068G>A (p.Pro1356=) rs115491049 0.00396
NM_032444.4(SLX4):c.336G>A (p.Pro112=) rs79126454 0.00393
NM_032444.4(SLX4):c.4600G>A (p.Gly1534Ser) rs78770603 0.00380
NM_032444.4(SLX4):c.1802C>T (p.Ser601Leu) rs59706816 0.00333
NM_032444.4(SLX4):c.3857C>T (p.Ala1286Val) rs149011965 0.00302
NM_032444.4(SLX4):c.4648C>T (p.Arg1550Trp) rs77021998 0.00214
NM_032444.4(SLX4):c.1163+10C>T rs80116508
NM_032444.4(SLX4):c.1164-75C>G rs59622164
NM_032444.4(SLX4):c.2161-299G>C rs111979605
NM_032444.4(SLX4):c.4739+79G>A rs74762428
NM_032444.4(SLX4):c.5154-80T>C rs75990295
NM_032444.4(SLX4):c.761-293T>G rs76743466

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