ClinVar Miner

List of variants in gene PRX reported by Genesis Genome Database

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_181882.3(PRX):c.3271G>A (p.Ala1091Thr) rs368459753 0.00008
NM_181882.3(PRX):c.1402G>A (p.Val468Met) rs763489447 0.00006
NM_181882.3(PRX):c.848T>G (p.Val283Gly) rs776556523 0.00005
NM_181882.3(PRX):c.2603A>G (p.Gln868Arg) rs1340773932 0.00003
NM_181882.3(PRX):c.716C>T (p.Pro239Leu) rs528907584 0.00003
NM_181882.3(PRX):c.2689C>T (p.Arg897Ter) rs756689732 0.00002
NM_181882.3(PRX):c.2707A>G (p.Ile903Val) rs941768924 0.00002
NM_181882.3(PRX):c.1102C>T (p.Arg368Ter) rs104894715 0.00001
NM_181882.3(PRX):c.2579A>C (p.Asp860Ala) rs759471716 0.00001
NM_181882.3(PRX):c.3208C>T (p.Arg1070Ter) rs104894708 0.00001
NM_181882.3(PRX):c.381+22C>A rs1316795222 0.00001
NM_181882.3(PRX):c.3925C>G (p.Pro1309Ala) rs754692947 0.00001
NM_181882.3(PRX):c.2611G>C (p.Val871Leu) rs754359052
NM_181882.3(PRX):c.2612T>C (p.Val871Ala) rs201389706
NM_181882.3(PRX):c.2615dup (p.Ala873fs) rs374001049
NM_181882.3(PRX):c.3722G>A (p.Gly1241Asp) rs139120811
NM_181882.3(PRX):c.379C>T (p.Leu127=) rs886054441
NM_181882.3(PRX):c.3873C>G (p.Tyr1291Ter) rs765769524
NM_181882.3(PRX):c.4186G>A (p.Asp1396Asn) rs566745894
NM_181882.3(PRX):c.4312C>G (p.Pro1438Ala) rs770666481
NM_181882.3(PRX):c.458del (p.Pro153fs) rs1599656851
NM_181882.3(PRX):c.862G>C (p.Val288Leu) rs568618329

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