ClinVar Miner

List of variants in gene PLA2G6 reported as uncertain significance for not specified

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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_003560.4(PLA2G6):c.101C>T (p.Ser34Leu) rs147948449 0.00040
NM_003560.4(PLA2G6):c.956C>T (p.Thr319Met) rs149653983 0.00029
NM_003560.4(PLA2G6):c.439G>A (p.Ala147Thr) rs138672490 0.00020
NM_003560.4(PLA2G6):c.386T>C (p.Leu129Pro) rs374746113 0.00019
NM_003560.4(PLA2G6):c.1835G>T (p.Arg612Leu) rs200117092 0.00018
NM_003560.4(PLA2G6):c.*19C>T rs377191625 0.00010
NM_003560.4(PLA2G6):c.209+6T>C rs376015031 0.00006
NM_003560.4(PLA2G6):c.1375C>T (p.Arg459Trp) rs753484966 0.00004
NM_003560.4(PLA2G6):c.1061T>C (p.Leu354Pro) rs1403125636 0.00001
NM_003560.4(PLA2G6):c.1501G>C (p.Glu501Gln) rs587784332 0.00001
NM_003560.4(PLA2G6):c.1898C>T (p.Ala633Val) rs201657455 0.00001
NM_003560.4(PLA2G6):c.1957G>A (p.Gly653Ser) rs754204295 0.00001
NM_003560.4(PLA2G6):c.1993A>G (p.Met665Val) rs1163553928 0.00001
NM_003560.4(PLA2G6):c.2364C>T (p.Tyr788=) rs748821599 0.00001
NM_003560.4(PLA2G6):c.1258G>A (p.Gly420Arg)
NM_003560.4(PLA2G6):c.1288C>T (p.Pro430Ser)
NM_003560.4(PLA2G6):c.1428-5T>G rs1555988730
NM_003560.4(PLA2G6):c.1506G>C (p.Lys502Asn) rs1555988382
NM_003560.4(PLA2G6):c.1511C>T (p.Ser504Leu)
NM_003560.4(PLA2G6):c.1547C>T (p.Ala516Val)
NM_003560.4(PLA2G6):c.1630A>C (p.Met544Leu)
NM_003560.4(PLA2G6):c.2159C>T (p.Thr720Ile)
NM_003560.4(PLA2G6):c.343C>T (p.Arg115Cys) rs995653548
NM_003560.4(PLA2G6):c.419TCA[1] (p.Ile141del)
NM_003560.4(PLA2G6):c.671T>C (p.Leu224Pro) rs2145803751
NM_003560.4(PLA2G6):c.692G>T (p.Gly231Val)
NM_003560.4(PLA2G6):c.920G>A (p.Gly307Asp)
NM_003560.4(PLA2G6):c.945_947dup (p.Ala316dup) rs797045889
NM_003560.4(PLA2G6):c.991G>A (p.Asp331Asn) rs199935023

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