ClinVar Miner

List of variants in gene PRRT2 reported as uncertain significance for not provided

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Gene type:
ClinVar version:
Total variants: 42
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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.1012G>A (p.Val338Met)
NM_145239.3(PRRT2):c.1013-29C>T rs745834081
NM_145239.3(PRRT2):c.1013T>C (p.Val338Ala) rs144540943
NM_145239.3(PRRT2):c.1016A>G (p.Tyr339Cys) rs1596895035
NM_145239.3(PRRT2):c.1020G>A (p.Lys340=) rs794727658
NM_145239.3(PRRT2):c.221C>A (p.Thr74Asn) rs1394261454
NM_145239.3(PRRT2):c.222C>G (p.Thr74=) rs1555502624
NM_145239.3(PRRT2):c.224C>T (p.Pro75Leu) rs147004110
NM_145239.3(PRRT2):c.239A>G (p.Glu80Gly) rs1064796466
NM_145239.3(PRRT2):c.281A>T (p.Glu94Val)
NM_145239.3(PRRT2):c.323_324del (p.Thr108fs) rs886041327
NM_145239.3(PRRT2):c.32T>G (p.Met11Arg) rs796052942
NM_145239.3(PRRT2):c.347A>T (p.Lys116Ile) rs201468618
NM_145239.3(PRRT2):c.352G>A (p.Ala118Thr) rs201636905
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.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.582G>C (p.Glu194Asp) rs794727310
NM_145239.3(PRRT2):c.618A>T (p.Lys206Asn) rs1555502715
NM_145239.3(PRRT2):c.619_621del (p.Lys207del) rs768603598
NM_145239.3(PRRT2):c.623C>T (p.Ser208Phe) rs201409113
NM_145239.3(PRRT2):c.640G>C (p.Ala214Pro) rs745594874
NM_145239.3(PRRT2):c.647C>T (p.Pro216Leu) rs76335820
NM_145239.3(PRRT2):c.67G>A (p.Glu23Lys) rs140383655
NM_145239.3(PRRT2):c.755C>G (p.Ala252Gly) rs1053144630
NM_145239.3(PRRT2):c.774G>T (p.Gly258=)
NM_145239.3(PRRT2):c.811C>G (p.Leu271Val) rs1596892978
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.866C>T (p.Ala289Val) rs1446585759
NM_145239.3(PRRT2):c.878T>G (p.Met293Arg) rs1555502804
NM_145239.3(PRRT2):c.879+6C>A rs201887920
NM_145239.3(PRRT2):c.880-20A>T rs727504110
NM_145239.3(PRRT2):c.912C>T (p.Asp304=) rs759633234
NM_145239.3(PRRT2):c.913G>A (p.Gly305Arg) rs767799831
NM_145239.3(PRRT2):c.916G>A (p.Ala306Thr) rs727504111
NM_145239.3(PRRT2):c.916G>T (p.Ala306Ser) rs727504111
NM_145239.3(PRRT2):c.931C>T (p.Arg311Trp) rs760521217

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