List of variants in gene SLX4 reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 37

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HGVS	dbSNP	gnomAD frequency
NM_032444.4(SLX4):c.90C>T (p.Ser30=)	rs118089506	0.00612
NM_032444.4(SLX4):c.1637A>G (p.Tyr546Cys)	rs150547487	0.00416
NM_032444.4(SLX4):c.4648C>T (p.Arg1550Trp)	rs77021998	0.00214
NM_032444.4(SLX4):c.2103G>C (p.Glu701Asp)	rs73505420	0.00210
NM_032444.4(SLX4):c.2328-9G>C	rs73505419	0.00188
NM_032444.4(SLX4):c.4024A>G (p.Ser1342Gly)	rs140051968	0.00141
NM_032444.4(SLX4):c.590T>C (p.Val197Ala)	rs147826749	0.00115
NM_032444.4(SLX4):c.4479G>A (p.Ser1493=)	rs150097733	0.00112
NM_032444.4(SLX4):c.339T>C (p.Ser113=)	rs144326379	0.00061
NM_032444.4(SLX4):c.3178C>T (p.Arg1060Trp)	rs144273492	0.00059
NM_032444.4(SLX4):c.2844G>A (p.Ala948=)	rs376877866	0.00053
NM_032444.4(SLX4):c.4836C>T (p.Asp1612=)	rs140844106	0.00051
NM_032444.4(SLX4):c.1707G>A (p.Pro569=)	rs141687678	0.00044
NM_032444.4(SLX4):c.467C>A (p.Thr156Lys)	rs144614070	0.00038
NM_032444.4(SLX4):c.1389A>G (p.Lys463=)	rs376668879	0.00019
NM_032444.4(SLX4):c.3583_3585del (p.Ile1195del)	rs199897550	0.00019
NM_032444.4(SLX4):c.5403G>C (p.Leu1801=)	rs577770118	0.00015
NM_032444.4(SLX4):c.2235C>T (p.Thr745=)	rs75184268	0.00012
NM_032444.4(SLX4):c.2241C>T (p.Ala747=)	rs143790956	0.00011
NM_032444.4(SLX4):c.4665C>T (p.Pro1555=)	rs749018784	0.00008
NM_032444.4(SLX4):c.1706C>T (p.Pro569Leu)	rs534528576	0.00007
NM_032444.4(SLX4):c.2034T>G (p.Val678=)	rs200278096	0.00007
NM_032444.4(SLX4):c.165C>T (p.Cys55=)	rs202030834	0.00006
NM_032444.4(SLX4):c.2424C>T (p.Cys808=)	rs774909246	0.00006
NM_032444.4(SLX4):c.4530G>T (p.Leu1510=)	rs139254595	0.00006
NM_032444.4(SLX4):c.2112C>T (p.Tyr704=)	rs566797597	0.00005
NM_032444.4(SLX4):c.2124C>T (p.Phe708=)	rs564042887	0.00003
NM_032444.4(SLX4):c.4485G>C (p.Ala1495=)	rs140872903	0.00003
NM_032444.4(SLX4):c.2055C>T (p.Val685=)	rs775934995	0.00002
NM_032444.4(SLX4):c.1026G>A (p.Pro342=)	rs755211335	0.00001
NM_032444.4(SLX4):c.1845C>T (p.Leu615=)	rs1056084	0.00001
NM_032444.4(SLX4):c.2421T>C (p.Asn807=)	rs760214045	0.00001
NM_032444.4(SLX4):c.2784C>T (p.Leu928=)	rs372754390	0.00001
NM_032444.4(SLX4):c.4383C>T (p.Ala1461=)	rs556719111	0.00001
NM_032444.4(SLX4):c.3621A>C (p.Pro1207=)	rs1436426423
NM_032444.4(SLX4):c.3900A>G (p.Glu1300=)	rs1060504341
NM_032444.4(SLX4):c.4596C>T (p.Ser1532=)	rs527733303

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