ClinVar Miner

List of variants in gene PCGF2 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 49
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_007144.3(PCGF2):c.377G>A (p.Ser126Asn) rs377546846 0.00009
NM_007144.3(PCGF2):c.333T>A (p.Asn111Lys) rs1320317505 0.00002
NM_007144.3(PCGF2):c.592G>A (p.Glu198Lys) rs568535028 0.00002
NM_007144.3(PCGF2):c.104T>A (p.Leu35Gln)
NM_007144.3(PCGF2):c.130G>A (p.Val44Met)
NM_007144.3(PCGF2):c.133C>T (p.Arg45Cys)
NM_007144.3(PCGF2):c.149A>G (p.Asn50Ser)
NM_007144.3(PCGF2):c.16C>T (p.Arg6Trp)
NM_007144.3(PCGF2):c.229G>A (p.Asp77Asn)
NM_007144.3(PCGF2):c.265+2T>C
NM_007144.3(PCGF2):c.267T>A (p.Asp89Glu)
NM_007144.3(PCGF2):c.275A>C (p.Lys92Thr)
NM_007144.3(PCGF2):c.304C>T (p.Pro102Ser)
NM_007144.3(PCGF2):c.307_308del (p.Leu103fs)
NM_007144.3(PCGF2):c.316+1G>T
NM_007144.3(PCGF2):c.319C>T (p.Pro107Ser)
NM_007144.3(PCGF2):c.323A>G (p.Asn108Ser) rs1906972407
NM_007144.3(PCGF2):c.325_326delinsAT (p.Gly109Ile)
NM_007144.3(PCGF2):c.343G>A (p.Gly115Ser)
NM_007144.3(PCGF2):c.344G>A (p.Gly115Asp)
NM_007144.3(PCGF2):c.361_363del (p.Glu121del)
NM_007144.3(PCGF2):c.367G>T (p.Gly123Trp) rs2143091509
NM_007144.3(PCGF2):c.374T>G (p.Leu125Arg)
NM_007144.3(PCGF2):c.384T>A (p.Asp128Glu)
NM_007144.3(PCGF2):c.391G>C (p.Val131Leu)
NM_007144.3(PCGF2):c.406G>A (p.Glu136Lys)
NM_007144.3(PCGF2):c.408A>C (p.Glu136Asp)
NM_007144.3(PCGF2):c.426-3C>T
NM_007144.3(PCGF2):c.430C>T (p.Arg144Trp)
NM_007144.3(PCGF2):c.439AAG[1] (p.Lys148del) rs2143088951
NM_007144.3(PCGF2):c.452T>C (p.Leu151Pro)
NM_007144.3(PCGF2):c.46C>T (p.Leu16Phe)
NM_007144.3(PCGF2):c.481-3C>G
NM_007144.3(PCGF2):c.483_484del (p.Val163fs)
NM_007144.3(PCGF2):c.487G>A (p.Val163Met)
NM_007144.3(PCGF2):c.491G>A (p.Arg164His)
NM_007144.3(PCGF2):c.520G>A (p.Val174Ile)
NM_007144.3(PCGF2):c.527A>C (p.His176Pro)
NM_007144.3(PCGF2):c.579G>A (p.Val193=)
NM_007144.3(PCGF2):c.583G>A (p.Val195Ile)
NM_007144.3(PCGF2):c.5A>C (p.His2Pro)
NM_007144.3(PCGF2):c.634G>A (p.Ala212Thr) rs1304683105
NM_007144.3(PCGF2):c.64G>T (p.Gly22Trp)
NM_007144.3(PCGF2):c.652C>T (p.Arg218Trp)
NM_007144.3(PCGF2):c.653G>A (p.Arg218Gln)
NM_007144.3(PCGF2):c.657+10C>T
NM_007144.3(PCGF2):c.82G>T (p.Ala28Ser)
NM_007144.3(PCGF2):c.8G>A (p.Arg3Gln)
NM_007144.3(PCGF2):c.94G>A (p.Val32Met)

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.