ClinVar Miner

List of variants in gene PRRT2 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 19
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HGVS dbSNP
NM_145239.3(PRRT2):c.-15dup rs1596889604
NM_145239.3(PRRT2):c.-30T>C rs202072359
NM_145239.3(PRRT2):c.-66+19G>A rs1000923002
NM_145239.3(PRRT2):c.1013-12C>T rs765953118
NM_145239.3(PRRT2):c.133C>T (p.Pro45Ser) rs11556732
NM_145239.3(PRRT2):c.201G>A (p.Leu67=) rs1416186042
NM_145239.3(PRRT2):c.225G>A (p.Pro75=) rs199662641
NM_145239.3(PRRT2):c.27T>G (p.Ser9=) rs1596889747
NM_145239.3(PRRT2):c.309C>T (p.Asp103=) rs772941122
NM_145239.3(PRRT2):c.37G>A (p.Gly13Arg) rs770164221
NM_145239.3(PRRT2):c.381G>A (p.Glu127=) rs747609927
NM_145239.3(PRRT2):c.417T>C (p.Ala139=) rs1596891097
NM_145239.3(PRRT2):c.642C>A (p.Ala214=) rs1237572544
NM_145239.3(PRRT2):c.647C>T (p.Pro216Leu) rs76335820
NM_145239.3(PRRT2):c.648C>G (p.Pro216=) rs772805935
NM_145239.3(PRRT2):c.912C>T (p.Asp304=) rs759633234
NM_145239.3(PRRT2):c.93A>G (p.Glu31=) rs1315799003
NM_145239.3(PRRT2):c.961C>T (p.Leu321=) rs756741951
NM_145239.3(PRRT2):c.99C>T (p.Gly33=) rs1235109136

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