List of variants in gene combination ATM, C11orf65 reported as uncertain significance for Breast and/or ovarian cancer

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: 33

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.6437G>C (p.Ser2146Thr)	rs56815840	0.00424
NM_000051.4(ATM):c.6860G>C (p.Gly2287Ala)	rs1800061	0.00096
NM_000051.4(ATM):c.7390T>C (p.Cys2464Arg)	rs55801750	0.00038
NM_000051.4(ATM):c.5821G>C (p.Val1941Leu)	rs147187700	0.00019
NM_000051.4(ATM):c.8734A>G (p.Arg2912Gly)	rs376676328	0.00019
NM_000051.4(ATM):c.7187C>G (p.Thr2396Ser)	rs370559102	0.00017
NM_000051.4(ATM):c.9086G>A (p.Gly3029Asp)	rs201199629	0.00016
NM_000051.4(ATM):c.8156G>A (p.Arg2719His)	rs55982963	0.00015
NM_000051.4(ATM):c.7618G>A (p.Val2540Ile)	rs35203200	0.00014
NM_000051.4(ATM):c.8560C>T (p.Arg2854Cys)	rs201958469	0.00013
NM_000051.4(ATM):c.5890A>G (p.Lys1964Glu)	rs201963507	0.00011
NM_000051.4(ATM):c.6343G>A (p.Val2115Ile)	rs587780634	0.00011
NM_000051.4(ATM):c.8495G>A (p.Arg2832His)	rs529296539	0.00006
NM_000051.4(ATM):c.8921C>T (p.Pro2974Leu)	rs139379666	0.00006
NM_000051.4(ATM):c.6604T>G (p.Tyr2202Asp)	rs730881311	0.00003
NM_000051.4(ATM):c.7375C>T (p.Arg2459Cys)	rs730881383	0.00003
NM_000051.4(ATM):c.7658C>A (p.Pro2553His)	rs864622368	0.00003
NM_000051.4(ATM):c.7999A>G (p.Met2667Val)	rs34099398	0.00003
NM_000051.4(ATM):c.8246A>T (p.Lys2749Ile)	rs779145081	0.00003
NM_000051.4(ATM):c.5971G>A (p.Glu1991Lys)	rs786203404	0.00001
NM_000051.4(ATM):c.6452+5T>A	rs533830556	0.00001
NM_000051.4(ATM):c.7871G>C (p.Cys2624Ser)	rs759392666	0.00001
NM_000051.4(ATM):c.8983C>A (p.Leu2995Ile)	rs142322668	0.00001
NM_000051.4(ATM):c.9128A>G (p.Lys3043Arg)	rs867893961	0.00001
NM_000051.4(ATM):c.6689T>C (p.Ile2230Thr)	rs587781562
NM_000051.4(ATM):c.6760C>T (p.His2254Tyr)	rs2136316772
NM_000051.4(ATM):c.6968G>A (p.Cys2323Tyr)	rs876660924
NM_000051.4(ATM):c.7858G>C (p.Val2620Leu)	rs1427723678
NM_000051.4(ATM):c.7976T>C (p.Leu2659Ser)	rs1565538536
NM_000051.4(ATM):c.8015A>C (p.Asp2672Ala)	rs763161651
NM_000051.4(ATM):c.8845G>A (p.Val2949Ile)	rs587782497
NM_000051.4(ATM):c.8851-10C>T	rs1057521676
NM_000051.4(ATM):c.9106A>G (p.Ile3036Val)	rs1565609567

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.