ClinVar Miner

List of variants in gene PSG2

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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_031246.4(PSG2):c.58G>C (p.Val20Leu) rs3887660 0.39093
NM_031246.4(PSG2):c.352G>C (p.Gly118Arg) rs149579909 0.07847
NM_031246.4(PSG2):c.31G>C (p.Glu11Gln) rs145433031 0.00067
NM_031246.4(PSG2):c.106G>A (p.Val36Ile) rs139102501 0.00026
NM_031246.4(PSG2):c.375A>G (p.Ile125Met) rs147024622 0.00017
NM_031246.4(PSG2):c.607T>G (p.Phe203Val) rs552740421 0.00012
NM_031246.4(PSG2):c.659G>A (p.Arg220Gln) rs372916591 0.00008
NM_031246.4(PSG2):c.940A>T (p.Thr314Ser) rs150464951 0.00008
NM_031246.4(PSG2):c.944C>T (p.Ser315Leu) rs749542888 0.00006
NM_031246.4(PSG2):c.367C>T (p.His123Tyr) rs375445497 0.00005
NM_031246.4(PSG2):c.87C>G (p.Asn29Lys) rs746907891 0.00005
NM_031246.4(PSG2):c.503C>T (p.Thr168Ile) rs772793169 0.00003
NM_031246.4(PSG2):c.626A>T (p.Lys209Met) rs550573659 0.00003
NM_031246.4(PSG2):c.682A>G (p.Ser228Gly) rs369117696 0.00003
NM_031246.4(PSG2):c.782G>T (p.Cys261Phe) rs548294601 0.00003
NM_031246.4(PSG2):c.16G>A (p.Ala6Thr) rs142061896 0.00001
NM_031246.4(PSG2):c.17C>A (p.Ala6Asp) rs780534792 0.00001
NM_031246.4(PSG2):c.224T>A (p.Leu75His) rs142667584 0.00001
NM_031246.4(PSG2):c.253G>C (p.Asp85His) rs774460898 0.00001
NM_031246.4(PSG2):c.274G>T (p.Gly92Trp) rs754245034 0.00001
NM_031246.4(PSG2):c.302C>T (p.Ala101Val) rs772237889 0.00001
NM_031246.4(PSG2):c.427T>C (p.Tyr143His) rs774584260 0.00001
NM_031246.4(PSG2):c.751T>A (p.Tyr251Asn) rs371852085 0.00001
NM_031246.4(PSG2):c.788C>T (p.Ala263Val) rs777210176 0.00001
NM_031246.4(PSG2):c.817T>C (p.Trp273Arg) rs2513497297 0.00001
NM_031246.4(PSG2):c.8C>T (p.Pro3Leu) rs748107642 0.00001
NM_031246.4(PSG2):c.94A>T (p.Thr32Ser) rs1263301392 0.00001
NM_031246.4(PSG2):c.113T>A (p.Ile38Asn)
NM_031246.4(PSG2):c.139G>A (p.Glu47Lys)
NM_031246.4(PSG2):c.164T>C (p.Val55Ala)
NM_031246.4(PSG2):c.216C>G (p.Ile72Met)
NM_031246.4(PSG2):c.247G>A (p.Val83Ile)
NM_031246.4(PSG2):c.254A>G (p.Asp85Gly)
NM_031246.4(PSG2):c.280G>C (p.Ala94Pro) rs1474011844
NM_031246.4(PSG2):c.280G>T (p.Ala94Ser) rs1474011844
NM_031246.4(PSG2):c.287G>C (p.Ser96Thr)
NM_031246.4(PSG2):c.293G>T (p.Arg98Leu) rs150218743
NM_031246.4(PSG2):c.301G>C (p.Ala101Pro) rs376555991
NM_031246.4(PSG2):c.310A>G (p.Asn104Asp) rs2513505334
NM_031246.4(PSG2):c.349G>A (p.Ala117Thr)
NM_031246.4(PSG2):c.356C>T (p.Ser119Phe)
NM_031246.4(PSG2):c.380G>A (p.Arg127Gln)
NM_031246.4(PSG2):c.41A>C (p.Lys14Thr)
NM_031246.4(PSG2):c.421A>T (p.Thr141Ser) rs1178866584
NM_031246.4(PSG2):c.422C>A (p.Thr141Asn) rs576799689
NM_031246.4(PSG2):c.42A>C (p.Lys14Asn)
NM_031246.4(PSG2):c.440C>A (p.Pro147His) rs771436678
NM_031246.4(PSG2):c.449C>A (p.Ser150Tyr) rs145532891
NM_031246.4(PSG2):c.52C>G (p.Leu18Val) rs147111943
NM_031246.4(PSG2):c.554A>G (p.Gln185Arg)
NM_031246.4(PSG2):c.563C>G (p.Pro188Arg)
NM_031246.4(PSG2):c.593C>T (p.Thr198Ile)
NM_031246.4(PSG2):c.610C>A (p.Leu204Ile) rs147461917
NM_031246.4(PSG2):c.610C>T (p.Leu204=) rs147461917
NM_031246.4(PSG2):c.649T>A (p.Cys217Ser)
NM_031246.4(PSG2):c.653A>T (p.Glu218Val) rs771616762
NM_031246.4(PSG2):c.679C>T (p.Arg227Cys)
NM_031246.4(PSG2):c.713G>T (p.Gly238Val) rs1393840390
NM_031246.4(PSG2):c.725C>G (p.Pro242Arg)
NM_031246.4(PSG2):c.742T>C (p.Tyr248His)
NM_031246.4(PSG2):c.745A>C (p.Thr249Pro)
NM_031246.4(PSG2):c.746C>A (p.Thr249Asn) rs144003252
NM_031246.4(PSG2):c.775T>G (p.Leu259Val)
NM_031246.4(PSG2):c.814T>C (p.Ser272Pro)
NM_031246.4(PSG2):c.847G>A (p.Gly283Arg) rs1272804761
NM_031246.4(PSG2):c.89T>C (p.Leu30Pro) rs758136893
NM_031246.4(PSG2):c.999T>A (p.Asn333Lys)

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