ClinVar Miner

List of variants in gene PRKCG reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002739.5(PRKCG):c.866C>A (p.Pro289Gln) rs376704133 0.00003
NM_002739.5(PRKCG):c.613C>T (p.Arg205Trp) rs367543208 0.00002
NM_002739.5(PRKCG):c.412G>A (p.Val138Met) rs1192424800 0.00001
NM_002739.5(PRKCG):c.745C>T (p.Arg249Trp) rs1180121813 0.00001
NM_002739.5(PRKCG):c.974C>T (p.Pro325Leu) rs145197557 0.00001
NM_002739.5(PRKCG):c.1055G>A (p.Ser352Asn) rs762206157
NM_002739.5(PRKCG):c.1081A>C (p.Ser361Arg) rs121918517
NM_002739.5(PRKCG):c.114C>T (p.Phe38=)
NM_002739.5(PRKCG):c.1192G>T (p.Val398Leu) rs1165667637
NM_002739.5(PRKCG):c.1195G>C (p.Glu399Gln) rs2068734193
NM_002739.5(PRKCG):c.1225G>C (p.Gly409Arg) rs1207949925
NM_002739.5(PRKCG):c.1290G>A (p.Leu430=)
NM_002739.5(PRKCG):c.1349G>A (p.Gly450Asp) rs2123016083
NM_002739.5(PRKCG):c.143T>C (p.Phe48Ser)
NM_002739.5(PRKCG):c.1553C>T (p.Thr518Ile) rs2068757477
NM_002739.5(PRKCG):c.1668T>G (p.Asp556Glu) rs1599954407
NM_002739.5(PRKCG):c.1706A>G (p.Glu569Gly) rs1461447265
NM_002739.5(PRKCG):c.1764+1G>A rs1406338491
NM_002739.5(PRKCG):c.1985T>C (p.Leu662Pro) rs1555808814
NM_002739.5(PRKCG):c.2004del (p.Asp669fs) rs1375924761
NM_002739.5(PRKCG):c.208_231del (p.Ser70_Cys77del) rs1599938583
NM_002739.5(PRKCG):c.221A>G (p.His74Arg) rs1568749767
NM_002739.5(PRKCG):c.229T>C (p.Cys77Arg) rs386134160
NM_002739.5(PRKCG):c.230G>A (p.Cys77Tyr) rs1599938631
NM_002739.5(PRKCG):c.254G>T (p.Cys85Phe) rs1599938680
NM_002739.5(PRKCG):c.362T>C (p.Leu121Pro) rs1568752907
NM_002739.5(PRKCG):c.362_379dup (p.Leu121_His126dup) rs2068657289
NM_002739.5(PRKCG):c.367G>C (p.Gly123Arg) rs386134164
NM_002739.5(PRKCG):c.382G>C (p.Gly128Arg) rs1568752939
NM_002739.5(PRKCG):c.392G>A (p.Cys131Tyr) rs386134167
NM_002739.5(PRKCG):c.415C>A (p.His139Asn) rs1555807019
NM_002739.5(PRKCG):c.425G>A (p.Cys142Tyr)
NM_002739.5(PRKCG):c.448T>C (p.Cys150Arg) rs1599943341
NM_002739.5(PRKCG):c.466G>A (p.Glu156Lys) rs1304701232
NM_002739.5(PRKCG):c.475G>A (p.Gly159Arg) rs866406014
NM_002739.5(PRKCG):c.476G>A (p.Gly159Glu) rs1599943390
NM_002739.5(PRKCG):c.479G>T (p.Arg160Leu) rs1555807032
NM_002739.5(PRKCG):c.495C>G (p.Ile165Met) rs1252158483
NM_002739.5(PRKCG):c.68G>A (p.Gly23Glu) rs1599937005
NM_002739.5(PRKCG):c.707T>C (p.Val236Ala) rs1599945617
NM_002739.5(PRKCG):c.70_72delinsCCT (p.Ala24Pro)
NM_002739.5(PRKCG):c.713G>A (p.Arg238His)
NM_002739.5(PRKCG):c.811G>A (p.Val271Met) rs375466358
NM_002739.5(PRKCG):c.866C>T (p.Pro289Leu) rs376704133
NM_002739.5(PRKCG):c.881A>T (p.Asp294Val)
NM_002739.5(PRKCG):c.8G>A (p.Gly3Asp)
NM_002739.5(PRKCG):c.99C>G (p.Val33=)

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.