List of variants in gene ATM reported as uncertain significance by Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center

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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.3925G>A (p.Ala1309Thr)	rs149711770	0.00081
NM_000051.4(ATM):c.4402G>A (p.Val1468Ile)	rs369903995	0.00034
NM_000051.4(ATM):c.4375G>A (p.Gly1459Arg)	rs145667735	0.00012
NM_000051.4(ATM):c.3175G>A (p.Ala1059Thr)	rs370282831	0.00004
NM_000051.4(ATM):c.2338A>T (p.Met780Leu)	rs587781446	0.00002
NM_000051.4(ATM):c.3743A>G (p.Tyr1248Cys)	rs766226370	0.00002
NM_000051.4(ATM):c.5053A>G (p.Thr1685Ala)	rs879254205
NM_000051.4(ATM):c.5232G>C (p.Lys1744Asn)	rs2083440178

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.