List of variants in gene ATR reported as uncertain significance for not specified

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: 24

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001184.4(ATR):c.2776T>C (p.Phe926Leu)	rs141783863	0.00119
NM_001184.4(ATR):c.7041+8G>A	rs201106004	0.00104
NM_001184.4(ATR):c.3424A>G (p.Ser1142Gly)	rs149008479	0.00058
NM_001184.4(ATR):c.6023G>T (p.Arg2008Leu)	rs145569221	0.00037
NM_001184.4(ATR):c.3581+5A>G	rs369917154	0.00029
NM_001184.4(ATR):c.1904G>A (p.Arg635Gln)	rs202162034	0.00027
NM_001184.4(ATR):c.5257A>G (p.Ile1753Val)	rs143806447	0.00021
NM_001184.4(ATR):c.1624A>G (p.Lys542Glu)	rs200491706	0.00006
NM_001184.4(ATR):c.1261A>G (p.Ser421Gly)	rs372973014	0.00005
NM_001184.4(ATR):c.3945+2dup	rs537031994	0.00004
NM_001184.4(ATR):c.5305G>C (p.Glu1769Gln)	rs376811787	0.00003
NM_001184.4(ATR):c.1626A>G (p.Lys542=)	rs762125386	0.00002
NM_001184.4(ATR):c.196G>A (p.Val66Met)	rs758564083	0.00001
NM_001184.4(ATR):c.2092G>A (p.Asp698Asn)	rs1553770633	0.00001
NC_000003.11:g.(?_142168076)_(142168445_142171969)del
NM_001184.4(ATR):c.2242A>G (p.Thr748Ala)	rs879255363
NM_001184.4(ATR):c.2327G>C (p.Ser776Thr)	rs979155439
NM_001184.4(ATR):c.3497A>C (p.His1166Pro)	rs201438783
NM_001184.4(ATR):c.3614A>G (p.His1205Arg)	rs1553767201
NM_001184.4(ATR):c.4626AGA[1] (p.Glu1543del)	rs755543843
NM_001184.4(ATR):c.5007T>C (p.Ile1669=)	rs2108361083
NM_001184.4(ATR):c.5739-11_5739-4del	rs797045404
NM_001184.4(ATR):c.6432A>G (p.Gln2144=)	rs376533466
NM_001184.4(ATR):c.7859T>C (p.Val2620Ala)	rs2108242274

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.