ClinVar Miner

List of variants in gene SLX4 reported as likely benign for DNA repair disease

Included ClinVar conditions (97):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 111
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HGVS dbSNP
NM_032444.4(SLX4):c.*1004A>G rs75773027
NM_032444.4(SLX4):c.*113C>T rs76661336
NM_032444.4(SLX4):c.*655G>A rs116003727
NM_032444.4(SLX4):c.*721T>C rs75146816
NM_032444.4(SLX4):c.*807G>A rs115690937
NM_032444.4(SLX4):c.*8A>G rs3751839
NM_032444.4(SLX4):c.*984C>T rs57699393
NM_032444.4(SLX4):c.-104A>G rs73505426
NM_032444.4(SLX4):c.-295A>G rs59311338
NM_032444.4(SLX4):c.-359C>G rs57910835
NM_032444.4(SLX4):c.1065G>A (p.Gln355=) rs200183071
NM_032444.4(SLX4):c.1152A>G (p.Pro384=) rs112511042
NM_032444.4(SLX4):c.1153C>A (p.Pro385Thr) rs115694169
NM_032444.4(SLX4):c.1156A>G (p.Met386Val) rs113490934
NM_032444.4(SLX4):c.1163+10C>T rs80116508
NM_032444.4(SLX4):c.1163+8G>A rs777094715
NM_032444.4(SLX4):c.1366+11T>C rs76350200
NM_032444.4(SLX4):c.1371T>G (p.Asn457Lys) rs74319927
NM_032444.4(SLX4):c.1389A>G (p.Lys463=) rs376668879
NM_032444.4(SLX4):c.1470C>T (p.Leu490=) rs139766312
NM_032444.4(SLX4):c.1662C>T (p.Leu554=) rs375996119
NM_032444.4(SLX4):c.1706C>T (p.Pro569Leu) rs534528576
NM_032444.4(SLX4):c.1707G>A (p.Pro569=) rs141687678
NM_032444.4(SLX4):c.1800G>A (p.Pro600=) rs777829533
NM_032444.4(SLX4):c.1803G>A (p.Ser601=) rs144892556
NM_032444.4(SLX4):c.1809G>A (p.Ser603=) rs565202250
NM_032444.4(SLX4):c.1896G>C (p.Gly632=) rs200859735
NM_032444.4(SLX4):c.1898G>A (p.Gly633Asp) rs1056085
NM_032444.4(SLX4):c.1911G>T (p.Ser637=) rs200013924
NM_032444.4(SLX4):c.192A>G (p.Lys64=) rs756720856
NM_032444.4(SLX4):c.1977G>A (p.Ser659=) rs572117922
NM_032444.4(SLX4):c.2012T>C (p.Leu671Ser) rs77985244
NM_032444.4(SLX4):c.2014-10_2014-8del rs759422070
NM_032444.4(SLX4):c.2022C>T (p.Leu674=) rs139900828
NM_032444.4(SLX4):c.2047G>A (p.Ala683Thr) rs115866745
NM_032444.4(SLX4):c.2055C>T (p.Val685=) rs775934995
NM_032444.4(SLX4):c.2103G>C (p.Glu701Asp) rs73505420
NM_032444.4(SLX4):c.2112C>T (p.Tyr704=) rs566797597
NM_032444.4(SLX4):c.2181C>T (p.Ser727=) rs565391485
NM_032444.4(SLX4):c.2193C>T (p.Asp731=) rs551541558
NM_032444.4(SLX4):c.2290C>G (p.Pro764Ala) rs151105762
NM_032444.4(SLX4):c.2359G>A (p.Glu787Lys) rs140600202
NM_032444.4(SLX4):c.2609C>T (p.Ala870Val) rs149584080
NM_032444.4(SLX4):c.2742T>C (p.Asp914=) rs1060504342
NM_032444.4(SLX4):c.2746G>T (p.Ala916Ser) rs79448721
NM_032444.4(SLX4):c.2748C>T (p.Ala916=) rs374815885
NM_032444.4(SLX4):c.2824G>C (p.Glu942Gln) rs114014006
NM_032444.4(SLX4):c.2850G>A (p.Glu950=) rs751882942
NM_032444.4(SLX4):c.2854G>A (p.Ala952Thr) rs59939128
NM_032444.4(SLX4):c.2855C>T (p.Ala952Val) rs78637028
NM_032444.4(SLX4):c.3012C>T (p.Pro1004=) rs533668167
NM_032444.4(SLX4):c.3108A>G (p.Leu1036=) rs751431046
NM_032444.4(SLX4):c.3162G>A (p.Ser1054=) rs76488917
NM_032444.4(SLX4):c.3178C>T (p.Arg1060Trp) rs144273492
NM_032444.4(SLX4):c.3180G>C (p.Arg1060=) rs747169328
NM_032444.4(SLX4):c.3189C>T (p.Gly1063=) rs200742809
NM_032444.4(SLX4):c.3367T>C (p.Ser1123Pro) rs201582780
NM_032444.4(SLX4):c.339T>C (p.Ser113=) rs144326379
NM_032444.4(SLX4):c.3438C>T (p.Asn1146=) rs78541095
NM_032444.4(SLX4):c.3583_3585del (p.Ile1195del) rs199897550
NM_032444.4(SLX4):c.3662C>T (p.Ala1221Val) rs3827530
NM_032444.4(SLX4):c.3663G>A (p.Ala1221=) rs760656992
NM_032444.4(SLX4):c.3676C>T (p.Arg1226Trp) rs142008398
NM_032444.4(SLX4):c.3738C>T (p.Ser1246=) rs376232540
NM_032444.4(SLX4):c.3774C>T (p.Pro1258=) rs146054214
NM_032444.4(SLX4):c.3782C>T (p.Pro1261Leu) rs374056556
NM_032444.4(SLX4):c.3783G>A (p.Pro1261=) rs77699867
NM_032444.4(SLX4):c.3801T>C (p.Arg1267=) rs772673695
NM_032444.4(SLX4):c.3812C>T (p.Ser1271Phe) rs3810813
NM_032444.4(SLX4):c.3868C>A (p.His1290Asn) rs112596894
NM_032444.4(SLX4):c.3900A>G (p.Glu1300=) rs1060504341
NM_032444.4(SLX4):c.3963G>A (p.Pro1321=) rs116781836
NM_032444.4(SLX4):c.4115G>A (p.Arg1372Gln) rs79174372
NM_032444.4(SLX4):c.4167G>A (p.Ala1389=) rs541433695
NM_032444.4(SLX4):c.422G>T (p.Gly141Val) rs77306735
NM_032444.4(SLX4):c.423G>A (p.Gly141=) rs111405249
NM_032444.4(SLX4):c.426T>A (p.Gly142=) rs377500336
NM_032444.4(SLX4):c.4335G>A (p.Arg1445=) rs139377113
NM_032444.4(SLX4):c.4338C>T (p.Thr1446=) rs77718962
NM_032444.4(SLX4):c.4347G>A (p.Leu1449=) rs373300793
NM_032444.4(SLX4):c.4371G>A (p.Arg1457=) rs745485209
NM_032444.4(SLX4):c.4383C>T (p.Ala1461=) rs556719111
NM_032444.4(SLX4):c.4456A>C (p.Arg1486=) rs200536796
NM_032444.4(SLX4):c.4485G>C (p.Ala1495=) rs140872903
NM_032444.4(SLX4):c.4494G>A (p.Leu1498=) rs146532299
NM_032444.4(SLX4):c.4545C>T (p.Asp1515=) rs142851654
NM_032444.4(SLX4):c.4581G>A (p.Pro1527=) rs78635099
NM_032444.4(SLX4):c.4600G>A (p.Gly1534Ser) rs78770603
NM_032444.4(SLX4):c.465A>G (p.Glu155=) rs138512851
NM_032444.4(SLX4):c.4665C>T (p.Pro1555=) rs749018784
NM_032444.4(SLX4):c.4686G>A (p.Pro1562=) rs752013105
NM_032444.4(SLX4):c.4716G>A (p.Pro1572=) rs372472816
NM_032444.4(SLX4):c.4836C>T (p.Asp1612=) rs140844106
NM_032444.4(SLX4):c.5106C>T (p.Ser1702=) rs1421905027
NM_032444.4(SLX4):c.5146T>A (p.Ser1716Thr) rs75182789
NM_032444.4(SLX4):c.5229G>A (p.Ser1743=) rs140231739
NM_032444.4(SLX4):c.5250G>A (p.Ala1750=) rs370495748
NM_032444.4(SLX4):c.5382G>A (p.Ser1794=) rs368848191
NM_032444.4(SLX4):c.5403G>C (p.Leu1801=) rs577770118
NM_032444.4(SLX4):c.5436C>T (p.Ala1812=) rs200473811
NM_032444.4(SLX4):c.5467C>A (p.Arg1823=) rs771230395
NM_032444.4(SLX4):c.555C>T (p.Asp185=) rs74640850
NM_032444.4(SLX4):c.590T>C (p.Val197Ala) rs147826749
NM_032444.4(SLX4):c.610C>T (p.Arg204Cys) rs79842542
NM_032444.4(SLX4):c.73G>A (p.Gly25Arg) rs201533738
NM_032444.4(SLX4):c.742G>A (p.Glu248Lys) rs148547201
NM_032444.4(SLX4):c.7C>T (p.Leu3=) rs751472980
NM_032444.4(SLX4):c.801G>A (p.Ala267=) rs375643423
NM_032444.4(SLX4):c.833G>A (p.Arg278Gln) rs201192909
NM_032444.4(SLX4):c.85C>T (p.Arg29Cys) rs144832924
NM_032444.4(SLX4):c.921C>T (p.Asn307=) rs370468973

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