ClinVar Miner

List of variants in gene SLX4 reported as likely benign for Fanconi anemia

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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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.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.1366+11T>C rs76350200
NM_032444.4(SLX4):c.1371T>G (p.Asn457Lys) rs74319927
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.1898G>A (p.Gly633Asp) rs1056085
NM_032444.4(SLX4):c.2012T>C (p.Leu671Ser) rs77985244
NM_032444.4(SLX4):c.2055C>T (p.Val685=) rs775934995
NM_032444.4(SLX4):c.2181C>T (p.Ser727=) rs565391485
NM_032444.4(SLX4):c.2609C>T (p.Ala870Val) rs149584080
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.3438C>T (p.Asn1146=) rs78541095
NM_032444.4(SLX4):c.3662C>T (p.Ala1221Val) rs3827530
NM_032444.4(SLX4):c.3783G>A (p.Pro1261=) rs77699867
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.3963G>A (p.Pro1321=) rs116781836
NM_032444.4(SLX4):c.4115G>A (p.Arg1372Gln) rs79174372
NM_032444.4(SLX4):c.423G>A (p.Gly141=) rs111405249
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.4581G>A (p.Pro1527=) rs78635099
NM_032444.4(SLX4):c.4600G>A (p.Gly1534Ser) rs78770603
NM_032444.4(SLX4):c.4716G>A (p.Pro1572=) rs372472816
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.5248G>T (p.Ala1750Ser)
NM_032444.4(SLX4):c.5249C>T (p.Ala1750Val)
NM_032444.4(SLX4):c.5382G>A (p.Ser1794=) rs368848191
NM_032444.4(SLX4):c.5436C>T (p.Ala1812=) rs200473811
NM_032444.4(SLX4):c.555C>T (p.Asp185=) rs74640850
NM_032444.4(SLX4):c.610C>T (p.Arg204Cys) rs79842542

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