List of variants in gene combination LOC129936899, PRKCD reported as uncertain significance for immune system disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
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.1981G>A (p.Ala661Thr)	rs149202171	0.00002
NM_006254.4(PRKCD):c.2003C>A (p.Pro668His)	rs782557014	0.00002
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.1873-3T>C	rs1703944773
NM_006254.4(PRKCD):c.1893T>G (p.Ser631Arg)
NM_006254.4(PRKCD):c.1926_1927delinsAT (p.Arg643Cys)
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

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.