List of variants in gene SLX4 reported as benign by PreventionGenetics, part of Exact Sciences

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: 40

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HGVS	dbSNP	gnomAD frequency
NM_032444.4(SLX4):c.4500T>C (p.Asn1500=)	rs3810812	0.63612
NM_032444.4(SLX4):c.753G>A (p.Ala251=)	rs8061528	0.21914
NM_032444.4(SLX4):c.3365C>T (p.Pro1122Leu)	rs714181	0.20566
NM_032444.4(SLX4):c.1366+11T>C	rs76350200	0.08654
NM_032444.4(SLX4):c.*8A>G	rs3751839	0.08334
NM_032444.4(SLX4):c.2854G>A (p.Ala952Thr)	rs59939128	0.07918
NM_032444.4(SLX4):c.2012T>C (p.Leu671Ser)	rs77985244	0.07388
NM_032444.4(SLX4):c.610C>T (p.Arg204Cys)	rs79842542	0.07023
NM_032444.4(SLX4):c.1371T>G (p.Asn457Lys)	rs74319927	0.06397
NM_032444.4(SLX4):c.1152A>G (p.Pro384=)	rs112511042	0.06386
NM_032444.4(SLX4):c.1156A>G (p.Met386Val)	rs113490934	0.06384
NM_032444.4(SLX4):c.2013+23G>A	rs112226642	0.06373
NM_032444.4(SLX4):c.2160+50C>T	rs75762935	0.06369
NM_032444.4(SLX4):c.555C>T (p.Asp185=)	rs74640850	0.04956
NM_032444.4(SLX4):c.2855C>T (p.Ala952Val)	rs78637028	0.04932
NM_032444.4(SLX4):c.3662C>T (p.Ala1221Val)	rs3827530	0.04930
NM_032444.4(SLX4):c.678C>T (p.His226=)	rs28516461	0.04916
NM_032444.4(SLX4):c.3812C>T (p.Ser1271Phe)	rs3810813	0.04718
NM_032444.4(SLX4):c.3162G>A (p.Ser1054=)	rs76488917	0.03405
NM_032444.4(SLX4):c.3783G>A (p.Pro1261=)	rs77699867	0.02290
NM_032444.4(SLX4):c.4581G>A (p.Pro1527=)	rs78635099	0.02283
NM_032444.4(SLX4):c.2824G>C (p.Glu942Gln)	rs114014006	0.01879
NM_032444.4(SLX4):c.3868C>A (p.His1290Asn)	rs112596894	0.01345
NM_032444.4(SLX4):c.1153C>A (p.Pro385Thr)	rs115694169	0.00968
NM_032444.4(SLX4):c.2746G>T (p.Ala916Ser)	rs79448721	0.00968
NM_032444.4(SLX4):c.4115G>A (p.Arg1372Gln)	rs79174372	0.00921
NM_032444.4(SLX4):c.5281C>T (p.Arg1761Cys)	rs143818824	0.00776
NM_032444.4(SLX4):c.3963G>A (p.Pro1321=)	rs116781836	0.00774
NM_032444.4(SLX4):c.2924C>T (p.Pro975Leu)	rs114472821	0.00679
NM_032444.4(SLX4):c.1803G>A (p.Ser601=)	rs144892556	0.00649
NM_032444.4(SLX4):c.1925-30G>A	rs149916101	0.00641
NM_032444.4(SLX4):c.1755C>T (p.Pro585=)	rs114016359	0.00638
NM_032444.4(SLX4):c.4068G>A (p.Pro1356=)	rs115491049	0.00396
NM_032444.4(SLX4):c.336G>A (p.Pro112=)	rs79126454	0.00393
NM_032444.4(SLX4):c.4600G>A (p.Gly1534Ser)	rs78770603	0.00380
NM_032444.4(SLX4):c.1802C>T (p.Ser601Leu)	rs59706816	0.00333
NM_032444.4(SLX4):c.4479G>A (p.Ser1493=)	rs150097733	0.00112
NM_032444.4(SLX4):c.3583_3585del (p.Ile1195del)	rs199897550	0.00019
NM_032444.4(SLX4):c.3315C>T (p.Ser1105=)	rs183029626	0.00015
NM_032444.4(SLX4):c.1163+10C>T	rs80116508

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