List of variants in gene ATM reported as likely benign by Natera, Inc.

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.544G>C (p.Val182Leu)	rs3218707	0.00757
NM_000051.4(ATM):c.3993+5G>T	rs3092842	0.00287
NM_000051.4(ATM):c.162T>C (p.Tyr54=)	rs3218690	0.00200
NM_000051.4(ATM):c.5071A>C (p.Ser1691Arg)	rs1800059	0.00169
NM_000051.4(ATM):c.1066-6T>G	rs201686625	0.00139
NM_000051.4(ATM):c.998C>T (p.Ser333Phe)	rs28904919	0.00137
NM_000051.4(ATM):c.4473C>T (p.Phe1491=)	rs4988008	0.00125
NM_000051.4(ATM):c.2127T>C (p.Ile709=)	rs56252953	0.00102
NM_000051.4(ATM):c.2289T>A (p.Phe763Leu)	rs34231402	0.00096
NM_000051.4(ATM):c.1744T>C (p.Phe582Leu)	rs2235006	0.00071
NM_000051.4(ATM):c.4424A>G (p.Tyr1475Cys)	rs34640941	0.00053
NM_000051.4(ATM):c.103C>A (p.Arg35=)	rs55861249	0.00032
NM_000051.4(ATM):c.1272T>C (p.Pro424=)	rs35578748	0.00019
NM_000051.4(ATM):c.3077+4G>A	rs201222237	0.00014
NM_000051.4(ATM):c.1773T>C (p.Asn591=)	rs61734356	0.00013
NM_000051.4(ATM):c.2346A>G (p.Leu782=)	rs730881285	0.00011
NM_000051.4(ATM):c.5005+7_5005+8del	rs587780626	0.00009
NM_000051.4(ATM):c.749G>A (p.Arg250Gln)	rs56123940	0.00007
NM_000051.4(ATM):c.1953A>G (p.Leu651=)	rs730881283	0.00004
NM_000051.4(ATM):c.2610C>T (p.Asn870=)	rs587780618	0.00004
NM_000051.4(ATM):c.1332C>A (p.Pro444=)	rs763361384	0.00003
NM_000051.4(ATM):c.1368A>G (p.Leu456=)	rs750579940	0.00003
NM_000051.4(ATM):c.3237T>C (p.Ala1079=)	rs564238520	0.00003
NM_000051.4(ATM):c.4674G>A (p.Thr1558=)	rs876658474	0.00003
NM_000051.4(ATM):c.2085G>A (p.Leu695=)	rs786202229	0.00002
NM_000051.4(ATM):c.3963G>A (p.Met1321Ile)	rs35184530	0.00002
NM_000051.4(ATM):c.660G>A (p.Ala220=)	rs763669136	0.00002
NM_000051.4(ATM):c.2577C>T (p.Asn859=)	rs730881286	0.00001
NM_000051.4(ATM):c.3577-7C>T	rs558667657	0.00001
NM_000051.4(ATM):c.15T>G (p.Leu5=)	rs1357506783
NM_000051.4(ATM):c.2031T>C (p.Ser677=)	rs1591534580
NM_000051.4(ATM):c.2754T>C (p.Phe918=)	rs758955717
NM_000051.4(ATM):c.2805G>C (p.Thr935=)	rs55934812
NM_000051.4(ATM):c.2805G>T (p.Thr935=)	rs55934812
NM_000051.4(ATM):c.5268A>T (p.Thr1756=)	rs1591708913

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