List of variants in gene ATM reported as likely benign by Genetic Services Laboratory, University of Chicago

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: 45

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.5557G>A (p.Asp1853Asn)	rs1801516	0.10783
NM_000051.4(ATM):c.378T>A (p.Asp126Glu)	rs2234997	0.06244
NM_000051.4(ATM):c.4578C>T (p.Pro1526=)	rs1800889	0.03133
NM_000051.4(ATM):c.657T>C (p.Cys219=)	rs2235003	0.02841
NM_000051.4(ATM):c.3118A>G (p.Met1040Val)	rs3092857	0.01233
NM_000051.4(ATM):c.4258C>T (p.Leu1420Phe)	rs1800058	0.01106
NM_000051.4(ATM):c.2362A>C (p.Ser788Arg)	rs641252	0.00242
NM_000051.4(ATM):c.162T>C (p.Tyr54=)	rs3218690	0.00200
NM_000051.4(ATM):c.370A>G (p.Ile124Val)	rs148590073	0.00198
NM_000051.4(ATM):c.1229T>C (p.Val410Ala)	rs56128736	0.00185
NM_000051.4(ATM):c.5071A>C (p.Ser1691Arg)	rs1800059	0.00169
NM_000051.4(ATM):c.609C>T (p.Asp203=)	rs144709948	0.00166
NM_000051.4(ATM):c.998C>T (p.Ser333Phe)	rs28904919	0.00133
NM_000051.4(ATM):c.4473C>T (p.Phe1491=)	rs4988008	0.00125
NM_000051.4(ATM):c.4388T>G (p.Phe1463Cys)	rs138327406	0.00098
NM_000051.4(ATM):c.3150T>C (p.Leu1050=)	rs3092859	0.00092
NM_000051.4(ATM):c.3925G>A (p.Ala1309Thr)	rs149711770	0.00081
NM_000051.4(ATM):c.3517T>C (p.Leu1173=)	rs141460670	0.00079
NM_000051.4(ATM):c.1744T>C (p.Phe582Leu)	rs2235006	0.00071
NM_000051.4(ATM):c.320G>A (p.Cys107Tyr)	rs142358238	0.00062
NM_000051.4(ATM):c.1986T>C (p.Phe662=)	rs1800055	0.00046
NM_000051.4(ATM):c.2932T>C (p.Ser978Pro)	rs139552233	0.00034
NM_000051.4(ATM):c.103C>A (p.Arg35=)	rs55861249	0.00032
NM_000051.4(ATM):c.3014A>G (p.Asn1005Ser)	rs146531614	0.00028
NM_000051.4(ATM):c.1272T>C (p.Pro424=)	rs35578748	0.00019
NM_000051.4(ATM):c.4980C>T (p.Asn1660=)	rs144338238	0.00017
NM_000051.4(ATM):c.4167A>G (p.Thr1389=)	rs183214437	0.00009
NM_000051.4(ATM):c.5005+7_5005+8del	rs587780626	0.00009
NM_000051.4(ATM):c.198A>G (p.Lys66=)	rs540920248	0.00006
NM_000051.4(ATM):c.2610C>T (p.Asn870=)	rs587780618	0.00004
NM_000051.4(ATM):c.3577-6G>A	rs56006345	0.00004
NM_000051.4(ATM):c.2040C>T (p.Phe680=)	rs587780855	0.00003
NM_000051.4(ATM):c.4437-9C>T	rs766003804	0.00002
NM_000051.4(ATM):c.4626G>A (p.Leu1542=)	rs786202784	0.00002
NM_000051.4(ATM):c.507T>C (p.Ser169=)	rs758619186	0.00002
NM_000051.4(ATM):c.2175C>T (p.Val725=)	rs140110298	0.00001
NM_000051.4(ATM):c.2922-8T>A	rs545892367	0.00001
NM_000051.4(ATM):c.4179C>A (p.Ile1393=)	rs775688446	0.00001
NM_000051.4(ATM):c.4416G>A (p.Leu1472=)	rs201526888	0.00001
NM_000051.4(ATM):c.5190A>G (p.Arg1730=)	rs786201609	0.00001
NM_000051.4(ATM):c.1380G>C (p.Thr460=)	rs145333518
NM_000051.4(ATM):c.2148C>G (p.Val716=)	rs1800701
NM_000051.4(ATM):c.2805G>C (p.Thr935=)	rs55934812
NM_000051.4(ATM):c.3154-4G>A	rs199543313
NM_000051.4(ATM):c.3403-13dup	rs3218681

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