ClinVar Miner

List of variants in gene SLX4 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP
NM_032444.4(SLX4):c.1153C>A (p.Pro385Thr) rs115694169
NM_032444.4(SLX4):c.1163+10C>G rs80116508
NM_032444.4(SLX4):c.1637A>G (p.Tyr546Cys) rs150547487
NM_032444.4(SLX4):c.1755C>T (p.Pro585=) rs114016359
NM_032444.4(SLX4):c.1802C>T (p.Ser601Leu) rs59706816
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.2034T>G (p.Val678=) rs200278096
NM_032444.4(SLX4):c.2235C>T (p.Thr745=) rs75184268
NM_032444.4(SLX4):c.231A>G (p.Gln77=) rs143279888
NM_032444.4(SLX4):c.2328-9G>C rs73505419
NM_032444.4(SLX4):c.2628C>T (p.Asp876=) rs201279467
NM_032444.4(SLX4):c.2746G>T (p.Ala916Ser) rs79448721
NM_032444.4(SLX4):c.2786C>T (p.Pro929Leu) rs117707719
NM_032444.4(SLX4):c.2824G>C (p.Glu942Gln) rs114014006
NM_032444.4(SLX4):c.2844G>A (p.Ala948=) rs376877866
NM_032444.4(SLX4):c.2854_2855delinsAT (p.Ala952Met) rs863224277
NM_032444.4(SLX4):c.2924C>T (p.Pro975Leu) rs114472821
NM_032444.4(SLX4):c.2975G>A (p.Gly992Glu) rs139287784
NM_032444.4(SLX4):c.3109T>C (p.Leu1037=) rs58735123
NM_032444.4(SLX4):c.3162G>A (p.Ser1054=) rs76488917
NM_032444.4(SLX4):c.3245A>G (p.Gln1082Arg) rs368657696
NM_032444.4(SLX4):c.3315C>T (p.Ser1105=) rs183029626
NM_032444.4(SLX4):c.3365C>T (p.Pro1122Leu) rs714181
NM_032444.4(SLX4):c.336G>A (p.Pro112=) rs79126454
NM_032444.4(SLX4):c.3662C>T (p.Ala1221Val) rs3827530
NM_032444.4(SLX4):c.3762G>A (p.Ser1254=) rs3810814
NM_032444.4(SLX4):c.3783G>A (p.Pro1261=) rs77699867
NM_032444.4(SLX4):c.3857C>T (p.Ala1286Val) rs149011965
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.4068G>A (p.Pro1356=) rs115491049
NM_032444.4(SLX4):c.4115G>A (p.Arg1372Gln) rs79174372
NM_032444.4(SLX4):c.4241C>T (p.Pro1414Leu) rs140892471
NM_032444.4(SLX4):c.4338C>T (p.Thr1446=) rs77718962
NM_032444.4(SLX4):c.4479G>A (p.Ser1493=) rs150097733
NM_032444.4(SLX4):c.4500T>C (p.Asn1500=) rs3810812
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.4648C>T (p.Arg1550Trp) rs77021998
NM_032444.4(SLX4):c.5029C>T (p.Pro1677Ser) rs7196345
NM_032444.4(SLX4):c.5146T>A (p.Ser1716Thr) rs75182789
NM_032444.4(SLX4):c.5259C>T (p.Asp1753=) rs144776083
NM_032444.4(SLX4):c.5281C>T (p.Arg1761Cys) rs143818824
NM_032444.4(SLX4):c.5501A>G (p.Asn1834Ser) rs111738042
NM_032444.4(SLX4):c.555C>T (p.Asp185=) rs74640850
NM_032444.4(SLX4):c.630A>G (p.Leu210=) rs746155183
NM_032444.4(SLX4):c.678C>T (p.His226=) rs28516461
NM_032444.4(SLX4):c.710G>A (p.Arg237Gln) rs138615800
NM_032444.4(SLX4):c.718A>G (p.Asn240Asp) rs114744903
NM_032444.4(SLX4):c.753G>A (p.Ala251=) rs8061528
NM_032444.4(SLX4):c.86G>A (p.Arg29His) rs149117119
NM_032444.4(SLX4):c.90C>T (p.Ser30=) rs118089506
NM_032444.4(SLX4):c.999C>T (p.Ile333=) rs7198338

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