ClinVar Miner

List of variants in gene PRMT7 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_019023.5(PRMT7):c.1714C>T (p.Arg572Cys) rs142409553 0.00015
NM_019023.5(PRMT7):c.499G>A (p.Val167Met) rs138763605 0.00007
NM_019023.5(PRMT7):c.-83-1G>A rs963987735 0.00003
NM_019023.5(PRMT7):c.1490G>A (p.Arg497Gln) rs753756119 0.00003
NM_019023.5(PRMT7):c.484G>A (p.Ala162Thr) rs764463683 0.00002
NM_019023.5(PRMT7):c.1436C>T (p.Pro479Leu) rs1441232897 0.00001
NM_019023.5(PRMT7):c.751G>A (p.Asp251Asn) rs770775042 0.00001
NM_019023.5(PRMT7):c.1126C>T (p.Arg376Trp)
NM_019023.5(PRMT7):c.1469A>G (p.Asn490Ser)
NM_019023.5(PRMT7):c.1951TTC[1] (p.Phe652del) rs562766169
NM_019023.5(PRMT7):c.2071C>T (p.Pro691Ser)
NM_019023.5(PRMT7):c.213TGGCAC[3] (p.Gly76_Leu77insThrGly) rs1169069876
NM_019023.5(PRMT7):c.320T>G (p.Val107Gly) rs2151557862
NM_019023.5(PRMT7):c.362A>G (p.Lys121Arg) rs753033088
NM_019023.5(PRMT7):c.374A>G (p.Glu125Gly) rs2151558937
NM_019023.5(PRMT7):c.524C>G (p.Pro175Arg) rs2544817988
NM_019023.5(PRMT7):c.796C>T (p.Arg266Trp)
NM_019023.5(PRMT7):c.964C>A (p.Pro322Thr)

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.