ClinVar Miner

List of variants in gene PRRT2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP
NM_145239.3(PRRT2):c.-15dup rs1596889604
NM_145239.3(PRRT2):c.-25G>C rs767022699
NM_145239.3(PRRT2):c.-32C>T rs777663292
NM_145239.3(PRRT2):c.-57G>A rs1057523086
NM_145239.3(PRRT2):c.-58C>T rs1057523156
NM_145239.3(PRRT2):c.-65-15CTC[2] rs1555502536
NM_145239.3(PRRT2):c.-65-28_-65-7dup rs1064796153
NM_145239.3(PRRT2):c.-66+19G>A rs1000923002
NM_145239.3(PRRT2):c.-88_-66+6del rs1555502431
NM_145239.3(PRRT2):c.1012+19C>T rs1057521417
NM_145239.3(PRRT2):c.1013-12C>T rs765953118
NM_145239.3(PRRT2):c.1013-16C>T rs539524685
NM_145239.3(PRRT2):c.1013T>C (p.Val338Ala) rs144540943
NM_145239.3(PRRT2):c.133C>T (p.Pro45Ser) rs11556732
NM_145239.3(PRRT2):c.171C>T (p.Ala57=) rs771487218
NM_145239.3(PRRT2):c.264C>T (p.Ser88=) rs752453955
NM_145239.3(PRRT2):c.309C>T (p.Asp103=) rs772941122
NM_145239.3(PRRT2):c.352G>A (p.Ala118Thr) rs201636905
NM_145239.3(PRRT2):c.357T>G (p.Thr119=) rs137942866
NM_145239.3(PRRT2):c.369G>T (p.Gly123=) rs1057521000
NM_145239.3(PRRT2):c.471A>G (p.Gln157=) rs763214510
NM_145239.3(PRRT2):c.519G>A (p.Glu173=) rs372588022
NM_145239.3(PRRT2):c.640G>C (p.Ala214Pro) rs745594874
NM_145239.3(PRRT2):c.644C>G (p.Pro215Arg) rs200926711
NM_145239.3(PRRT2):c.645C>T (p.Pro215=) rs183683129
NM_145239.3(PRRT2):c.647C>A (p.Pro216His) rs76335820
NM_145239.3(PRRT2):c.647C>G (p.Pro216Arg) rs76335820
NM_145239.3(PRRT2):c.66C>T (p.Gly22=) rs775756146
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.773G>A (p.Gly258Glu) rs560303559
NM_145239.3(PRRT2):c.828C>T (p.Cys276=) rs35625748
NM_145239.3(PRRT2):c.834C>T (p.Cys278=) rs758654999
NM_145239.3(PRRT2):c.879+20A>G rs1555502808
NM_145239.3(PRRT2):c.879+6C>A rs201887920
NM_145239.3(PRRT2):c.87A>G (p.Glu29=) rs1057521028
NM_145239.3(PRRT2):c.880-13G>A rs377384734
NM_145239.3(PRRT2):c.912C>T (p.Asp304=) rs759633234
NM_145239.3(PRRT2):c.936A>T (p.Val312=) rs1057520864

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