List of variants in gene ATM reported as likely benign by Counsyl

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: 36

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.735C>T (p.Val245=)	rs3218674	0.01085
NM_000051.4(ATM):c.2572T>C (p.Phe858Leu)	rs1800056	0.00861
NM_000051.4(ATM):c.2119T>C (p.Ser707Pro)	rs4986761	0.00782
NM_000051.4(ATM):c.3383A>G (p.Gln1128Arg)	rs2229020	0.00636
NM_000051.4(ATM):c.5558A>T (p.Asp1853Val)	rs1801673	0.00441
NM_000051.4(ATM):c.2362A>C (p.Ser788Arg)	rs641252	0.00265
NM_000051.4(ATM):c.370A>G (p.Ile124Val)	rs148590073	0.00215
NM_000051.4(ATM):c.1229T>C (p.Val410Ala)	rs56128736	0.00186
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.4388T>G (p.Phe1463Cys)	rs138327406	0.00103
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.4612-32_4612-30del	rs113149503	0.00031
NM_000051.4(ATM):c.3403-16_3403-15insA	rs569564716	0.00016
NM_000051.4(ATM):c.2220A>G (p.Ala740=)	rs56353517	0.00005
NM_000051.4(ATM):c.2919A>G (p.Leu973=)	rs587779829	0.00005
NM_000051.4(ATM):c.5005+14A>T	rs374337879	0.00005
NM_000051.4(ATM):c.3378A>G (p.Lys1126=)	rs149182949	0.00004
NM_000051.4(ATM):c.3577-6G>A	rs56006345	0.00004
NM_000051.4(ATM):c.4332G>A (p.Leu1444=)	rs753570046	0.00002
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.192A>G (p.Leu64=)	rs587780616	0.00001
NM_000051.4(ATM):c.2639-7T>C	rs912886321	0.00001
NM_000051.4(ATM):c.3336T>A (p.Pro1112=)	rs758784434	0.00001
NM_000051.4(ATM):c.4149G>A (p.Ser1383=)	rs749180334	0.00001
NM_000051.4(ATM):c.4236+8T>C	rs765636697	0.00001
NM_000051.4(ATM):c.4436+10A>G	rs878853509	0.00001
NM_000051.4(ATM):c.1020C>A (p.Ala340=)	rs546927781
NM_000051.4(ATM):c.2805G>C (p.Thr935=)	rs55934812
NM_000051.4(ATM):c.2839-18dup	rs730881287
NM_000051.4(ATM):c.4776+23_4776+25del	rs770860526
NM_000051.4(ATM):c.5145G>A (p.Leu1715=)	rs786202765
NM_000051.4(ATM):c.5178-11G>A	rs200876654
NM_000051.4(ATM):c.5497-9A>G	rs878853524

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