ClinVar Miner

List of variants in gene LOC129936899, PRKCD studied for type IV hypersensitivity disease

Included ClinVar conditions (21):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 28
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HGVS dbSNP gnomAD frequency
NM_006254.4(PRKCD):c.1926G>A (p.Ala642=) rs56338517 0.03080
NM_006254.4(PRKCD):c.1928G>A (p.Arg643His) rs369041593 0.00011
NM_006254.4(PRKCD):c.1927C>T (p.Arg643Cys) rs778015441 0.00008
NM_006254.4(PRKCD):c.1956C>T (p.Ile652=) rs147565728 0.00006
NM_006254.4(PRKCD):c.1981G>A (p.Ala661Thr) rs149202171 0.00002
NM_006254.4(PRKCD):c.2003C>A (p.Pro668His) rs782557014 0.00002
NM_006254.4(PRKCD):c.2010C>T (p.Phe670=) rs781808423 0.00002
NM_006254.4(PRKCD):c.2028T>C (p.Asp676=) rs782403404 0.00002
NM_006254.4(PRKCD):c.1941C>T (p.Ser647=) rs781997779 0.00001
NM_006254.4(PRKCD):c.1942G>A (p.Asp648Asn) rs1305829710 0.00001
NM_006254.4(PRKCD):c.1957G>A (p.Asp653Asn) rs781914241 0.00001
NM_006254.4(PRKCD):c.2002C>T (p.Pro668Ser) rs148364495 0.00001
NM_006254.4(PRKCD):c.1873-19C>T
NM_006254.4(PRKCD):c.1873-20C>T
NM_006254.4(PRKCD):c.1873-3T>C rs1703944773
NM_006254.4(PRKCD):c.1881C>G (p.Pro627=) rs199634315
NM_006254.4(PRKCD):c.1881C>T (p.Pro627=)
NM_006254.4(PRKCD):c.1893T>G (p.Ser631Arg)
NM_006254.4(PRKCD):c.1917C>T (p.Asn639=)
NM_006254.4(PRKCD):c.1926_1927delinsAT (p.Arg643Cys)
NM_006254.4(PRKCD):c.1944C>T (p.Asp648=)
NM_006254.4(PRKCD):c.1980C>T (p.Phe660=)
NM_006254.4(PRKCD):c.1998G>A (p.Val666=) rs1575547280
NM_006254.4(PRKCD):c.2001C>T (p.Asn667=)
NM_006254.4(PRKCD):c.2016C>A (p.His672Gln) rs1553671108
NM_006254.4(PRKCD):c.2024A>G (p.Glu675Gly)
NM_006254.4(PRKCD):c.2026G>T (p.Asp676Tyr) rs2107293780
NM_006254.4(PRKCD):c.2030G>T (p.Ter677Leu) rs2107293797

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