List of variants in gene SLX4 reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 96

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HGVS	dbSNP	gnomAD frequency
NM_032444.4(SLX4):c.1637A>G (p.Tyr546Cys)	rs150547487	0.00416
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.3676C>T (p.Arg1226Trp)	rs142008398	0.00114
NM_032444.4(SLX4):c.2047G>A (p.Ala683Thr)	rs115866745	0.00092
NM_032444.4(SLX4):c.1372A>G (p.Lys458Glu)	rs149126845	0.00087
NM_032444.4(SLX4):c.85C>T (p.Arg29Cys)	rs144832924	0.00078
NM_032444.4(SLX4):c.4261A>T (p.Ile1421Phe)	rs141567438	0.00069
NM_032444.4(SLX4):c.2756C>T (p.Thr919Ile)	rs145533919	0.00052
NM_032444.4(SLX4):c.2975G>A (p.Gly992Glu)	rs139287784	0.00049
NM_032444.4(SLX4):c.2249C>T (p.Thr750Met)	rs145353518	0.00046
NM_032444.4(SLX4):c.2654C>T (p.Pro885Leu)	rs147492092	0.00036
NM_032444.4(SLX4):c.2681T>G (p.Val894Gly)	rs145137472	0.00036
NM_032444.4(SLX4):c.4384G>T (p.Ala1462Ser)	rs138484365	0.00034
NM_032444.4(SLX4):c.3368C>A (p.Ser1123Tyr)	rs144647122	0.00031
NM_032444.4(SLX4):c.2210G>A (p.Arg737His)	rs146901714	0.00029
NM_032444.4(SLX4):c.1394C>T (p.Pro465Leu)	rs372128800	0.00024
NM_032444.4(SLX4):c.742G>A (p.Glu248Lys)	rs148547201	0.00024
NM_032444.4(SLX4):c.1499C>T (p.Thr500Met)	rs377440877	0.00019
NM_032444.4(SLX4):c.5264C>T (p.Ala1755Val)	rs372921011	0.00019
NM_032444.4(SLX4):c.4580C>T (p.Pro1527Leu)	rs149362820	0.00018
NM_032444.4(SLX4):c.537G>T (p.Glu179Asp)	rs758789462	0.00017
NM_032444.4(SLX4):c.3940C>A (p.Gln1314Lys)	rs142040192	0.00016
NM_032444.4(SLX4):c.*1T>C	rs559903847	0.00014
NM_032444.4(SLX4):c.832C>T (p.Arg278Trp)	rs141597706	0.00014
NM_032444.4(SLX4):c.2160+8C>T	rs374004875	0.00011
NM_032444.4(SLX4):c.2437G>A (p.Glu813Lys)	rs770020510	0.00011
NM_032444.4(SLX4):c.3648G>T (p.Gln1216His)	rs139544666	0.00010
NM_032444.4(SLX4):c.73G>A (p.Gly25Arg)	rs201533738	0.00010
NM_032444.4(SLX4):c.1223G>A (p.Arg408Gln)	rs377135500	0.00009
NM_032444.4(SLX4):c.2006G>A (p.Arg669His)	rs200807331	0.00009
NM_032444.4(SLX4):c.2005C>T (p.Arg669Cys)	rs375524355	0.00007
NM_032444.4(SLX4):c.2753C>T (p.Thr918Ile)	rs781323142	0.00006
NM_032444.4(SLX4):c.3068C>A (p.Ala1023Asp)	rs769271628	0.00006
NM_032444.4(SLX4):c.5072A>G (p.Asn1691Ser)	rs551385115	0.00006
NM_032444.4(SLX4):c.996G>T (p.Gln332His)	rs377201471	0.00006
NM_032444.4(SLX4):c.1379G>A (p.Arg460His)	rs369994733	0.00005
NM_032444.4(SLX4):c.2259C>G (p.His753Gln)	rs374294258	0.00005
NM_032444.4(SLX4):c.4046G>C (p.Gly1349Ala)	rs151144102	0.00005
NM_032444.4(SLX4):c.5476C>T (p.Arg1826Trp)	rs199736788	0.00005
NM_032444.4(SLX4):c.1583G>A (p.Ser528Asn)	rs752899329	0.00004
NM_032444.4(SLX4):c.3782C>T (p.Pro1261Leu)	rs374056556	0.00004
NM_032444.4(SLX4):c.4964G>A (p.Arg1655Lys)	rs149726415	0.00004
NM_032444.4(SLX4):c.800C>T (p.Ala267Val)	rs752160984	0.00004
NM_032444.4(SLX4):c.1547C>T (p.Ala516Val)	rs199683722	0.00003
NM_032444.4(SLX4):c.2940C>T (p.Ala980=)	rs1415684146	0.00003
NM_032444.4(SLX4):c.3062G>C (p.Arg1021Pro)	rs200842643	0.00003
NM_032444.4(SLX4):c.349G>T (p.Ala117Ser)	rs775853263	0.00003
NM_032444.4(SLX4):c.3799C>T (p.Arg1267Cys)	rs201422743	0.00003
NM_032444.4(SLX4):c.485C>T (p.Thr162Met)	rs140876043	0.00003
NM_032444.4(SLX4):c.5263G>T (p.Ala1755Ser)	rs780678810	0.00003
NM_032444.4(SLX4):c.708G>A (p.Ala236=)	rs765742613	0.00003
NM_032444.4(SLX4):c.922G>A (p.Val308Met)	rs775151113	0.00003
NM_032444.4(SLX4):c.2843C>T (p.Ala948Val)	rs781462011	0.00002
NM_032444.4(SLX4):c.401C>T (p.Ala134Val)	rs759574554	0.00002
NM_032444.4(SLX4):c.5242C>T (p.Gln1748Ter)	rs776789371	0.00002
NM_032444.4(SLX4):c.5423T>G (p.Phe1808Cys)	rs371390105	0.00002
NM_032444.4(SLX4):c.1034C>A (p.Thr345Asn)	rs751770341	0.00001
NM_032444.4(SLX4):c.1493C>T (p.Ser498Phe)	rs1326014010	0.00001
NM_032444.4(SLX4):c.1603G>A (p.Ala535Thr)	rs776394340	0.00001
NM_032444.4(SLX4):c.2118C>T (p.His706=)	rs371401752	0.00001
NM_032444.4(SLX4):c.3370A>G (p.Ile1124Val)	rs766081510	0.00001
NM_032444.4(SLX4):c.4604G>A (p.Gly1535Glu)	rs1425908713	0.00001
NM_032444.4(SLX4):c.4897A>G (p.Thr1633Ala)	rs771698300	0.00001
NM_032444.4(SLX4):c.107A>T (p.Glu36Val)	rs370082083
NM_032444.4(SLX4):c.1141AGC[2] (p.Ser383del)	rs938490986
NM_032444.4(SLX4):c.1405C>T (p.Pro469Ser)	rs763833617
NM_032444.4(SLX4):c.1511C>G (p.Pro504Arg)	rs569591337
NM_032444.4(SLX4):c.1569T>C (p.Pro523=)	rs2151131241
NM_032444.4(SLX4):c.1672C>A (p.Arg558=)	rs372264472
NM_032444.4(SLX4):c.1672C>T (p.Arg558Trp)	rs372264472
NM_032444.4(SLX4):c.1732G>C (p.Glu578Gln)	rs1202254236
NM_032444.4(SLX4):c.1799C>A (p.Pro600Gln)	rs749277750
NM_032444.4(SLX4):c.1929G>C (p.Leu643Phe)
NM_032444.4(SLX4):c.2057A>G (p.Asn686Ser)	rs571330689
NM_032444.4(SLX4):c.2336T>C (p.Val779Ala)	rs1555450482
NM_032444.4(SLX4):c.2615G>A (p.Gly872Asp)
NM_032444.4(SLX4):c.3122A>G (p.Gln1041Arg)	rs1384033342
NM_032444.4(SLX4):c.3209C>G (p.Ser1070Cys)	rs2040570774
NM_032444.4(SLX4):c.32G>T (p.Gly11Val)	rs1555452514
NM_032444.4(SLX4):c.3902G>T (p.Gly1301Val)	rs1307466531
NM_032444.4(SLX4):c.4057C>A (p.His1353Asn)	rs142205392
NM_032444.4(SLX4):c.4134G>C (p.Pro1378=)	rs760757846
NM_032444.4(SLX4):c.421G>T (p.Gly141Trp)	rs137976282
NM_032444.4(SLX4):c.422G>C (p.Gly141Ala)	rs77306735
NM_032444.4(SLX4):c.4374G>A (p.Met1458Ile)	rs1168844302
NM_032444.4(SLX4):c.4465C>G (p.Gln1489Glu)	rs2151121176
NM_032444.4(SLX4):c.4546G>C (p.Gly1516Arg)	rs775915651
NM_032444.4(SLX4):c.4739+5G>A	rs879255425
NM_032444.4(SLX4):c.4808_4809delinsCT (p.His1603Pro)
NM_032444.4(SLX4):c.506C>T (p.Ser169Leu)	rs776018346
NM_032444.4(SLX4):c.5262G>A (p.Glu1754=)	rs1158728649
NM_032444.4(SLX4):c.577T>C (p.Leu193=)	rs760477564
NM_032444.4(SLX4):c.611G>A (p.Arg204His)
NM_032444.4(SLX4):c.822G>C (p.Gln274His)	rs1367038373

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