ClinVar Miner

List of variants studied for Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 102
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HGVS dbSNP gnomAD frequency
NM_006513.4(SARS1):c.1160G>A (p.Gly387Glu) rs140717526 0.00927
NM_006513.4(SARS1):c.1387+8T>C rs74854256 0.00920
NM_017827.4(SARS2):c.273G>A (p.Ser91=) rs144229840 0.00672
NM_017827.4(SARS2):c.364-14C>T rs150151686 0.00412
NM_017827.4(SARS2):c.963-17T>C rs201465773 0.00136
NM_017827.4(SARS2):c.696C>T (p.Arg232=) rs35389151 0.00118
NM_017827.4(SARS2):c.576C>T (p.Val192=) rs150249937 0.00048
NM_017827.4(SARS2):c.17C>T (p.Ala6Val) rs201988841 0.00029
NM_017827.4(SARS2):c.91A>C (p.Arg31=) rs138274440 0.00025
NM_017827.4(SARS2):c.-5C>A rs376534605 0.00015
NM_017827.4(SARS2):c.353G>A (p.Arg118Gln) rs377601567 0.00015
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.136G>A (p.Glu46Lys) rs142446687 0.00012
NM_017827.4(SARS2):c.1292G>A (p.Arg431His) rs146193366 0.00010
NM_017827.4(SARS2):c.1348-19G>A rs540813245 0.00009
NM_017827.4(SARS2):c.1501A>G (p.Ile501Val) rs776562420 0.00009
NM_017827.4(SARS2):c.988C>T (p.Arg330Trp) rs781367675 0.00009
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.540C>T (p.Val180=) rs371250326 0.00006
NM_017827.4(SARS2):c.795C>T (p.Arg265=) rs372151812 0.00003
NM_017827.4(SARS2):c.230G>T (p.Arg77Leu) rs902727059 0.00002
NM_017827.4(SARS2):c.534+9C>T rs200404554 0.00002
NM_017827.4(SARS2):c.796G>A (p.Gly266Arg) rs767412508 0.00002
NM_017827.4(SARS2):c.1205G>A (p.Arg402His) rs370842354 0.00001
NM_017827.4(SARS2):c.30G>A (p.Trp10Ter) rs145754412 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.759+4T>C rs749164566 0.00001
NM_017827.4(SARS2):c.1004C>T (p.Thr335Met)
NM_017827.4(SARS2):c.1019G>A (p.Arg340Gln)
NM_017827.4(SARS2):c.1031G>C (p.Arg344Pro)
NM_017827.4(SARS2):c.1084G>T (p.Glu362Ter)
NM_017827.4(SARS2):c.1091G>A (p.Ser364Asn)
NM_017827.4(SARS2):c.1161-11C>T
NM_017827.4(SARS2):c.1238G>A (p.Arg413Gln)
NM_017827.4(SARS2):c.1244G>A (p.Arg415His)
NM_017827.4(SARS2):c.1294C>T (p.Arg432Cys)
NM_017827.4(SARS2):c.1295G>A (p.Arg432His)
NM_017827.4(SARS2):c.1318G>A (p.Glu440Lys)
NM_017827.4(SARS2):c.1387G>T (p.Ala463Ser)
NM_017827.4(SARS2):c.1388C>T (p.Ala463Val)
NM_017827.4(SARS2):c.1400G>A (p.Ser467Asn)
NM_017827.4(SARS2):c.1417G>A (p.Gly473Ser)
NM_017827.4(SARS2):c.1432C>T (p.Pro478Ser)
NM_017827.4(SARS2):c.1439C>T (p.Ala480Val)
NM_017827.4(SARS2):c.1454T>A (p.Leu485His)
NM_017827.4(SARS2):c.1456G>A (p.Gly486Ser)
NM_017827.4(SARS2):c.1468A>T (p.Ile490Phe)
NM_017827.4(SARS2):c.146G>A (p.Arg49His)
NM_017827.4(SARS2):c.1493T>C (p.Leu498Pro)
NM_017827.4(SARS2):c.1537G>A (p.Gly513Ser)
NM_017827.4(SARS2):c.1546G>T (p.Ala516Ser)
NM_017827.4(SARS2):c.154T>C (p.Tyr52His)
NM_017827.4(SARS2):c.15G>A (p.Met5Ile)
NM_017827.4(SARS2):c.166C>G (p.Pro56Ala)
NM_017827.4(SARS2):c.176A>C (p.Asp59Ala)
NM_017827.4(SARS2):c.201A>T (p.Pro67=)
NM_017827.4(SARS2):c.223del (p.Glu75fs)
NM_017827.4(SARS2):c.244C>G (p.Arg82Gly)
NM_017827.4(SARS2):c.279G>A (p.Trp93Ter)
NM_017827.4(SARS2):c.344A>G (p.Glu115Gly)
NM_017827.4(SARS2):c.363+6C>T
NM_017827.4(SARS2):c.415C>T (p.Arg139Trp)
NM_017827.4(SARS2):c.427C>G (p.Arg143Gly)
NM_017827.4(SARS2):c.428G>A (p.Arg143Gln)
NM_017827.4(SARS2):c.454C>A (p.Leu152Met)
NM_017827.4(SARS2):c.455T>A (p.Leu152Gln)
NM_017827.4(SARS2):c.476T>A (p.Leu159His)
NM_017827.4(SARS2):c.485A>G (p.Gln162Arg)
NM_017827.4(SARS2):c.500C>T (p.Ala167Val)
NM_017827.4(SARS2):c.50G>A (p.Gly17Glu)
NM_017827.4(SARS2):c.532G>A (p.Val178Met)
NM_017827.4(SARS2):c.559C>T (p.Arg187Ter)
NM_017827.4(SARS2):c.55C>G (p.Arg19Gly)
NM_017827.4(SARS2):c.565C>T (p.Leu189Phe)
NM_017827.4(SARS2):c.589+1del
NM_017827.4(SARS2):c.613C>T (p.His205Tyr)
NM_017827.4(SARS2):c.649C>A (p.Gln217Lys)
NM_017827.4(SARS2):c.653+2_653+3del
NM_017827.4(SARS2):c.667G>A (p.Val223Met)
NM_017827.4(SARS2):c.679C>A (p.Arg227=)
NM_017827.4(SARS2):c.679C>T (p.Arg227Trp) rs761305168
NM_017827.4(SARS2):c.680G>A (p.Arg227Gln)
NM_017827.4(SARS2):c.695G>A (p.Arg232His)
NM_017827.4(SARS2):c.701C>T (p.Ala234Val)
NM_017827.4(SARS2):c.744C>A (p.Asn248Lys)
NM_017827.4(SARS2):c.755G>A (p.Arg252His)
NM_017827.4(SARS2):c.759+3A>G
NM_017827.4(SARS2):c.793C>T (p.Arg265Cys)
NM_017827.4(SARS2):c.826C>A (p.Pro276Thr)
NM_017827.4(SARS2):c.829A>G (p.Asn277Asp)
NM_017827.4(SARS2):c.837C>A (p.Asn279Lys)
NM_017827.4(SARS2):c.839C>T (p.Pro280Leu)
NM_017827.4(SARS2):c.858C>G (p.Ile286Met)
NM_017827.4(SARS2):c.889G>T (p.Ala297Ser)
NM_017827.4(SARS2):c.916+16G>A
NM_017827.4(SARS2):c.916+1G>A
NM_017827.4(SARS2):c.934A>G (p.Thr312Ala)
NM_017827.4(SARS2):c.937G>A (p.Val313Met)
NM_017827.4(SARS2):c.940G>T (p.Ala314Ser)

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