ClinVar Miner

List of variants in gene MPP2 reported as uncertain significance by Ambry Genetics

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_005374.5(MPP2):c.236C>T (p.Ala79Val) rs148439699 0.00013
NM_005374.5(MPP2):c.1031G>A (p.Arg344His) rs141122901 0.00010
NM_005374.5(MPP2):c.1180C>T (p.Arg394Trp) rs371532689 0.00003
NM_005374.5(MPP2):c.1499G>A (p.Arg500Gln) rs761519494 0.00003
NM_005374.5(MPP2):c.401C>T (p.Pro134Leu) rs1317497694 0.00003
NM_005374.5(MPP2):c.592C>T (p.Arg198Cys) rs752282662 0.00003
NM_005374.5(MPP2):c.1210C>T (p.Arg404Cys) rs374234227 0.00002
NM_005374.5(MPP2):c.1045C>T (p.Arg349Cys) rs758838631 0.00001
NM_005374.5(MPP2):c.1048C>T (p.Arg350Trp) rs935555535 0.00001
NM_005374.5(MPP2):c.1294G>A (p.Asp432Asn) rs764271151 0.00001
NM_005374.5(MPP2):c.1378G>A (p.Glu460Lys) rs762561901 0.00001
NM_005374.5(MPP2):c.1528C>T (p.Arg510Trp) rs1400882581 0.00001
NM_005374.5(MPP2):c.613C>T (p.Arg205Cys) rs544561497 0.00001
NM_005374.5(MPP2):c.677G>A (p.Arg226His) rs543947750 0.00001
NM_005374.5(MPP2):c.1093A>G (p.Ser365Gly)
NM_005374.5(MPP2):c.1119G>C (p.Trp373Cys)
NM_005374.5(MPP2):c.122A>G (p.Glu41Gly) rs772606038
NM_005374.5(MPP2):c.1270G>T (p.Gly424Cys)
NM_005374.5(MPP2):c.1280A>T (p.Tyr427Phe)
NM_005374.5(MPP2):c.1310T>C (p.Val437Ala)
NM_005374.5(MPP2):c.1313T>C (p.Val438Ala) rs2509059164
NM_005374.5(MPP2):c.1448C>A (p.Ala483Glu) rs1241458957
NM_005374.5(MPP2):c.1529G>A (p.Arg510Gln)
NM_005374.5(MPP2):c.1562T>A (p.Val521Asp)
NM_005374.5(MPP2):c.1564A>G (p.Asn522Asp)
NM_005374.5(MPP2):c.1591G>A (p.Glu531Lys)
NM_005374.5(MPP2):c.226C>T (p.Arg76Trp)
NM_005374.5(MPP2):c.316A>C (p.Thr106Pro) rs2509080327
NM_005374.5(MPP2):c.488T>C (p.Val163Ala)
NM_005374.5(MPP2):c.698A>G (p.His233Arg)
NM_005374.5(MPP2):c.725G>A (p.Ser242Asn)
NM_005374.5(MPP2):c.725G>C (p.Ser242Thr)
NM_005374.5(MPP2):c.916T>C (p.Ser306Pro) rs2509068966
NM_005374.5(MPP2):c.931G>A (p.Gly311Ser) rs200915083

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