ClinVar Miner

List of variants in gene PRRT2 reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_145239.3(PRRT2):c.-65-2dup rs1555502538
NM_145239.3(PRRT2):c.-66+1G>A rs796052939
NM_145239.3(PRRT2):c.1011C>T (p.Gly337=) rs745970212
NM_145239.3(PRRT2):c.221C>A (p.Thr74Asn) rs1394261454
NM_145239.3(PRRT2):c.239A>G (p.Glu80Gly) rs1064796466
NM_145239.3(PRRT2):c.32T>G (p.Met11Arg) rs796052942
NM_145239.3(PRRT2):c.415G>A (p.Ala139Thr) rs763634807
NM_145239.3(PRRT2):c.431C>T (p.Pro144Leu) rs1317648011
NM_145239.3(PRRT2):c.455C>A (p.Pro152His) rs760278435
NM_145239.3(PRRT2):c.460C>T (p.Pro154Ser) rs571941412
NM_145239.3(PRRT2):c.522T>G (p.Ser174Arg) rs777955072
NM_145239.3(PRRT2):c.580G>A (p.Glu194Lys) rs139516010
NM_145239.3(PRRT2):c.603C>G (p.His201Gln) rs543313284
NM_145239.3(PRRT2):c.623C>T (p.Ser208Phe) rs201409113
NM_145239.3(PRRT2):c.638G>A (p.Gly213Glu) rs796052935
NM_145239.3(PRRT2):c.85G>A (p.Glu29Lys) rs1555502574
NM_145239.3(PRRT2):c.864C>A (p.Phe288Leu) rs1359563519
NM_145239.3(PRRT2):c.878T>G (p.Met293Arg) rs1555502804
NM_145239.3(PRRT2):c.916G>T (p.Ala306Ser) rs727504111
NM_145239.3(PRRT2):c.931C>T (p.Arg311Trp) rs760521217
NM_145239.3(PRRT2):c.979ATC[2] (p.Ile329del) rs1057518374

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