ClinVar Miner

List of variants in gene PRRT2 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 93
Download table as spreadsheet
HGVS dbSNP
NM_145239.3(PRRT2):c.-15dup rs1596889604
NM_145239.3(PRRT2):c.-25G>C rs767022699
NM_145239.3(PRRT2):c.-30T>C rs202072359
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.1012+7G>A
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.1020G>A (p.Lys340=) rs794727658
NM_145239.3(PRRT2):c.115G>A (p.Ala39Thr)
NM_145239.3(PRRT2):c.133C>T (p.Pro45Ser) rs11556732
NM_145239.3(PRRT2):c.144G>A (p.Pro48=)
NM_145239.3(PRRT2):c.15C>T (p.Ser5=)
NM_145239.3(PRRT2):c.171C>T (p.Ala57=) rs771487218
NM_145239.3(PRRT2):c.183A>G (p.Ser61=) rs775396962
NM_145239.3(PRRT2):c.192G>A (p.Lys64=)
NM_145239.3(PRRT2):c.201G>A (p.Leu67=) rs1416186042
NM_145239.3(PRRT2):c.222C>G (p.Thr74=) rs1555502624
NM_145239.3(PRRT2):c.225G>A (p.Pro75=) rs199662641
NM_145239.3(PRRT2):c.264C>T (p.Ser88=) rs752453955
NM_145239.3(PRRT2):c.279G>A (p.Gly93=) rs1596890586
NM_145239.3(PRRT2):c.27T>G (p.Ser9=) rs1596889747
NM_145239.3(PRRT2):c.299G>A (p.Ser100Asn) rs1596890680
NM_145239.3(PRRT2):c.303C>T (p.Pro101=) rs570325174
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.354C>T (p.Ala118=)
NM_145239.3(PRRT2):c.357T>G (p.Thr119=) rs137942866
NM_145239.3(PRRT2):c.364C>A (p.Gln122Lys) rs1555502665
NM_145239.3(PRRT2):c.369G>T (p.Gly123=) rs1057521000
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.39G>A (p.Gly13=)
NM_145239.3(PRRT2):c.412C>G (p.Pro138Ala) rs79182085
NM_145239.3(PRRT2):c.417T>C (p.Ala139=) rs1596891097
NM_145239.3(PRRT2):c.418C>T (p.Pro140Ser)
NM_145239.3(PRRT2):c.432C>T (p.Pro144=) rs749031499
NM_145239.3(PRRT2):c.435G>T (p.Arg145=)
NM_145239.3(PRRT2):c.471A>G (p.Gln157=) rs763214510
NM_145239.3(PRRT2):c.483T>C (p.Pro161=) rs751980660
NM_145239.3(PRRT2):c.519G>A (p.Glu173=) rs372588022
NM_145239.3(PRRT2):c.528G>A (p.Gly176=) rs749569594
NM_145239.3(PRRT2):c.564G>A (p.Gln188=) rs545201760
NM_145239.3(PRRT2):c.580G>A (p.Glu194Lys) rs139516010
NM_145239.3(PRRT2):c.612C>G (p.Pro204=) rs149260055
NM_145239.3(PRRT2):c.623C>A (p.Ser208Tyr) rs201409113
NM_145239.3(PRRT2):c.624C>T (p.Ser208=)
NM_145239.3(PRRT2):c.640G>C (p.Ala214Pro) rs745594874
NM_145239.3(PRRT2):c.642C>A (p.Ala214=) rs1237572544
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.647C>T (p.Pro216Leu) rs76335820
NM_145239.3(PRRT2):c.648C>G (p.Pro216=) rs772805935
NM_145239.3(PRRT2):c.648C>T (p.Pro216=) rs772805935
NM_145239.3(PRRT2):c.651A>G (p.Arg217=)
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.702G>A (p.Gly234=)
NM_145239.3(PRRT2):c.708A>G (p.Pro236=)
NM_145239.3(PRRT2):c.709G>A (p.Gly237Arg) rs199556853
NM_145239.3(PRRT2):c.723T>C (p.Gly241=)
NM_145239.3(PRRT2):c.753G>A (p.Leu251=)
NM_145239.3(PRRT2):c.755C>G (p.Ala252Gly) rs1053144630
NM_145239.3(PRRT2):c.772G>C (p.Gly258Arg) rs996840274
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.855C>T (p.Ile285=)
NM_145239.3(PRRT2):c.879+10A>G
NM_145239.3(PRRT2):c.879+20A>G rs1555502808
NM_145239.3(PRRT2):c.879+6C>A rs201887920
NM_145239.3(PRRT2):c.879+8C>T
NM_145239.3(PRRT2):c.87A>G (p.Glu29=) rs1057521028
NM_145239.3(PRRT2):c.880-10C>T
NM_145239.3(PRRT2):c.880-13G>A rs377384734
NM_145239.3(PRRT2):c.880-5C>T
NM_145239.3(PRRT2):c.912C>T (p.Asp304=) rs759633234
NM_145239.3(PRRT2):c.936A>T (p.Val312=) rs1057520864
NM_145239.3(PRRT2):c.93A>G (p.Glu31=) rs1315799003
NM_145239.3(PRRT2):c.945C>G (p.Leu315=)
NM_145239.3(PRRT2):c.961C>T (p.Leu321=) rs756741951
NM_145239.3(PRRT2):c.990C>T (p.Ala330=) rs1322978278
NM_145239.3(PRRT2):c.996C>T (p.Cys332=)
NM_145239.3(PRRT2):c.99C>T (p.Gly33=) rs1235109136

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.