List of variants in gene SARS2 reported as uncertain significance for Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome

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: 48

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HGVS	dbSNP	gnomAD frequency
NM_017827.4(SARS2):c.310C>T (p.Arg104Trp)	rs144760517	0.00518
NM_017827.4(SARS2):c.390G>A (p.Gln130=)	rs61736057	0.00233
NM_017827.4(SARS2):c.*22C>T	rs199819134	0.00080
NM_017827.4(SARS2):c.364-7C>A	rs528674259	0.00066
NM_017827.4(SARS2):c.501G>A (p.Ala167=)	rs140304897	0.00063
NM_017827.3(SARS2):c.*341G>C	rs374281807	0.00039
NM_017827.4(SARS2):c.590-5T>A	rs370612303	0.00035
NM_017827.4(SARS2):c.1315A>T (p.Thr439Ser)	rs200202461	0.00029
NM_017827.4(SARS2):c.1347+10G>A	rs376335678	0.00019
NM_017827.4(SARS2):c.654-11C>G	rs200300920	0.00017
NM_017827.4(SARS2):c.353G>A (p.Arg118Gln)	rs377601567	0.00015
NM_017827.4(SARS2):c.1317C>T (p.Thr439=)	rs556892787	0.00013
NM_017827.4(SARS2):c.1404C>A (p.Asn468Lys)	rs369183237	0.00013
NM_017827.4(SARS2):c.448G>A (p.Val150Ile)	rs143847153	0.00013
NM_017827.4(SARS2):c.1292G>A (p.Arg431His)	rs146193366	0.00010
NM_017827.4(SARS2):c.988C>T (p.Arg330Trp)	rs781367675	0.00009
NM_017827.4(SARS2):c.637G>A (p.Asp213Asn)	rs151116675	0.00008
NM_017827.4(SARS2):c.*140C>T	rs565577459	0.00007
NM_017827.4(SARS2):c.758G>A (p.Arg253Gln)	rs185053576	0.00007
NM_017827.4(SARS2):c.1291C>T (p.Arg431Cys)	rs752872984	0.00006
NM_017827.4(SARS2):c.1428C>T (p.Leu476=)	rs372552234	0.00004
NM_017827.4(SARS2):c.888G>A (p.Leu296=)	rs182484523	0.00004
NM_017827.4(SARS2):c.917-4C>T	rs542117712	0.00004
NM_017827.4(SARS2):c.900G>A (p.Ala300=)	rs144529043	0.00003
NM_017827.4(SARS2):c.963-10T>C	rs749126576	0.00003
NM_017827.4(SARS2):c.589+4G>A	rs772644235	0.00002
NM_017827.4(SARS2):c.796G>A (p.Gly266Arg)	rs767412508	0.00002
NM_017827.4(SARS2):c.*131C>T	rs558549222	0.00001
NM_017827.4(SARS2):c.*224C>T	rs763374780	0.00001
NM_017827.4(SARS2):c.*250A>G	rs377325293	0.00001
NM_017827.4(SARS2):c.1205G>A (p.Arg402His)	rs370842354	0.00001
NM_017827.4(SARS2):c.1321G>A (p.Ala441Thr)	rs762422369	0.00001
NM_017827.4(SARS2):c.315C>G (p.Ser105Arg)	rs1300533578	0.00001
NM_017827.4(SARS2):c.373G>A (p.Asp125Asn)	rs771968331	0.00001
NM_017827.4(SARS2):c.446T>C (p.Leu149Pro)	rs762785941	0.00001
NM_017827.4(SARS2):c.534+10G>A	rs531462148	0.00001
NM_017827.4(SARS2):c.759+4T>C	rs749164566	0.00001
NM_017827.4(SARS2):c.777G>A (p.Thr259=)	rs563299553	0.00001
NM_017827.4(SARS2):c.*22C>A	rs199819134
NM_017827.4(SARS2):c.1481C>T (p.Thr494Ile)	rs138608193
NM_017827.4(SARS2):c.394-5C>G	rs886054429
NM_017827.4(SARS2):c.535-15G>C	rs886054428
NM_017827.4(SARS2):c.655C>T (p.Arg219Cys)
NM_017827.4(SARS2):c.679C>T (p.Arg227Trp)	rs761305168
NM_017827.4(SARS2):c.794G>C (p.Arg265Pro)	rs760416819
NM_017827.4(SARS2):c.820A>T (p.Met274Leu)	rs1974461797
NM_017827.4(SARS2):c.862C>T (p.Pro288Ser)	rs1033683967
NM_017827.4(SARS2):c.877G>A (p.Asp293Asn)	rs917884456

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