ClinVar Miner

List of variants in gene PRKCD reported as benign for autoimmune disease

Included ClinVar conditions (82):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_006254.4(PRKCD):c.1857T>C (p.Pro619=) rs900495 0.94337
NM_006254.4(PRKCD):c.1782C>G (p.Thr594=) rs1075865 0.93819
NM_006254.4(PRKCD):c.1441C>T (p.Leu481=) rs2306574 0.75510
NM_006254.4(PRKCD):c.1743+29T>G rs7630600 0.74353
NM_006254.4(PRKCD):c.115+21C>G rs2306571 0.65337
NM_006254.4(PRKCD):c.1119G>A (p.Glu373=) rs2230494 0.29106
NM_006254.4(PRKCD):c.180T>C (p.Asp60=) rs2230493 0.12323
NM_006254.4(PRKCD):c.1260+19G>A rs41275531 0.10858
NM_006254.4(PRKCD):c.741C>T (p.Cys247=) rs55709737 0.00741
NM_006254.4(PRKCD):c.214G>C (p.Val72Leu) rs151061939 0.00535
NM_006254.4(PRKCD):c.1554+8G>A rs141412493 0.00429
NM_006254.4(PRKCD):c.1260+6C>T rs180706867 0.00270
NM_006254.4(PRKCD):c.603C>T (p.Ile201=) rs75794462 0.00108
NM_006254.4(PRKCD):c.1415+19C>T rs202080219 0.00105
NM_006254.4(PRKCD):c.315+9C>A rs200076653 0.00078
NM_006254.4(PRKCD):c.1043A>G (p.Asn348Ser) rs33911937 0.00064
NM_006254.4(PRKCD):c.539+13C>T rs200442846 0.00058
NM_006254.4(PRKCD):c.1743+8C>T rs182290450 0.00038
NM_006254.4(PRKCD):c.1299G>A (p.Gly433=) rs200890839 0.00008
NM_006254.4(PRKCD):c.115+14C>G rs781949983 0.00004
NM_006254.4(PRKCD):c.658-9del
NM_006254.4(PRKCD):c.912A>G (p.Ser304=) rs529176751

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