ClinVar Miner

List of variants reported for not provided by Institute of Human Genetics, University of Leipzig Medical Center

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003977.4(AIP):c.911G>A (p.Arg304Gln) rs104894190 0.00115
NM_000546.6(TP53):c.892del (p.Glu298fs) rs2073177507
NM_014168.4(METTL5):c.571_572del (p.Lys191fs) rs1573965358
NM_015275.3(WASHC4):c.3041A>G (p.Tyr1014Cys) rs768574664

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.