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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 490407	NM_000051.4(ATM):c.-18G>A	ATM	Single nucleotide variant (5 prime UTR variant)	not specified +2 more	GBenign/Likely benign
Select item 181944	NM_000051.4(ATM):c.76G>C (p.Glu26Gln)	ATM (E26Q)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 186439	NM_000051.4(ATM):c.78A>T (p.Glu26Asp)	ATM (E26D)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +4 more	GUncertain significance
Select item 3048	NM_000051.4(ATM):c.146C>G (p.Ser49Cys)	ATM (S49C)	Single nucleotide variant (missense variant)	Familial cancer of breast	GBenign FDA Recognized database
Select item 132757	NM_000051.4(ATM):c.162T>C (p.Tyr54=)	ATM	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 127341	NM_000051.4(ATM):c.170G>A (p.Trp57Ter)	ATM (W57*)	Single nucleotide variant (nonsense)	Ataxia-telangiectasia syndrome +4 more	GPathogenic
Select item 489518	NM_000051.4(ATM):c.186-17A>G	ATM	Single nucleotide variant (intron variant)	Familial cancer of breast +6 more	GBenign
Select item 135737	NM_000051.4(ATM):c.186-7C>T	ATM	Single nucleotide variant (intron variant)	Breast and/or ovarian cancer +6 more	GBenign/Likely benign
Select item 127373	NM_000051.4(ATM):c.370A>G (p.Ile124Val)	ATM (I124V)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 185849	NM_000051.4(ATM):c.372C>A (p.Ile124=)	ATM	Single nucleotide variant (synonymous variant)	ATM-related condition +4 more	GBenign/Likely benign
Select item 128455	NM_000051.4(ATM):c.378T>A (p.Asp126Glu)	ATM (D126E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GBenign/Likely benign
Select item 994243	NM_000051.4(ATM):c.380C>T (p.Thr127Ile)	ATM (T127I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 141546	NM_000051.4(ATM):c.381del (p.Thr127_Val128insTer)	ATM	Deletion (frameshift variant)	Familial cancer of breast +4 more	GPathogenic/Likely pathogenic
Select item 618539	NM_000051.4(ATM):c.502T>C (p.Phe168Leu)	ATM (F168L)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 132685	NM_000051.4(ATM):c.544G>C (p.Val182Leu)	ATM (V182L)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +5 more	GBenign/Likely benign
Select item 135764	NM_000051.4(ATM):c.609C>T (p.Asp203=)	ATM	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 133639	NM_000051.4(ATM):c.649A>G (p.Ile217Val)	ATM (I217V)	Single nucleotide variant (missense variant)	not specified +5 more	GUncertain significance
Select item 186210	NM_000051.4(ATM):c.712A>G (p.Ile238Val)	ATM (I238V)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 183707	NM_000051.4(ATM):c.735C>T (p.Val245=)	ATM	Single nucleotide variant (synonymous variant)	Ataxia-telangiectasia syndrome +5 more	GBenign/Likely benign
Select item 127471	NM_000051.4(ATM):c.998C>T (p.Ser333Phe)	ATM (S333F)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +6 more	GConflicting classifications of pathogenicity
Select item 3038	NM_000051.4(ATM):c.1066-6T>G	ATM	Single nucleotide variant (intron variant)	Familial cancer of breast	GBenign FDA Recognized database
Select item 142140	NM_000051.4(ATM):c.1176C>G (p.Gly392=)	ATM	Single nucleotide variant (synonymous variant)	Familial cancer of breast	GBenign FDA Recognized database
Select item 127332	NM_000051.4(ATM):c.1229T>C (p.Val410Ala)	ATM (V410A)	Single nucleotide variant (missense variant)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 584777	NM_000051.4(ATM):c.1236G>T (p.Trp412Cys)	ATM (W412C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 132714	NM_000051.4(ATM):c.1254A>G (p.Gln418=)	ATM	Single nucleotide variant (synonymous variant)	Familial cancer of breast +6 more	GBenign/Likely benign
Select item 481277	NM_000051.4(ATM):c.1314A>C (p.Ile438=)	ATM	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 184641	NM_000051.4(ATM):c.1332C>A (p.Pro444=)	ATM	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 133602	NM_000051.4(ATM):c.1541G>A (p.Gly514Asp)	ATM (G514D)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +6 more	GBenign/Likely benign
Select item 133604	NM_000051.4(ATM):c.1636C>G (p.Leu546Val)	ATM (L546V)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +6 more	GBenign/Likely benign
Select item 421483	NM_000051.4(ATM):c.1726A>G (p.Ile576Val)	ATM (I576V)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 136435	NM_000051.4(ATM):c.1773T>C (p.Asn591=)	ATM	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 127343	NM_000051.4(ATM):c.1810C>T (p.Pro604Ser)	ATM (P604S)	Single nucleotide variant (missense variant)	Hereditary breast ovarian cancer syndrome +7 more	GConflicting classifications of pathogenicity
Select item 453393	NM_000051.4(ATM):c.1899-55T>G	ATM	Single nucleotide variant (intron variant)	Ataxia-telangiectasia syndrome +3 more	GBenign
Select item 135740	NM_000051.4(ATM):c.1986T>C (p.Phe662=)	ATM	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 185505	NM_000051.4(ATM):c.2085G>A (p.Leu695=)	ATM	Single nucleotide variant (synonymous variant)	Ataxia-telangiectasia syndrome +4 more	GBenign/Likely benign
Select item 128454	NM_000051.4(ATM):c.2119T>C (p.Ser707Pro)	ATM (S707P)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign
Select item 185153	NM_000051.4(ATM):c.2148C>G (p.Val716=)	ATM	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 140761	NM_000051.4(ATM):c.2193C>T (p.Tyr731=)	ATM	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +6 more	GBenign/Likely benign
Select item 181926	NM_000051.4(ATM):c.2251-10T>G	ATM	Single nucleotide variant (intron variant)	Ataxia-telangiectasia syndrome +3 more	GConflicting classifications of pathogenicity
Select item 127349	NM_000051.4(ATM):c.2362A>C (p.Ser788Arg)	ATM (S788R)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +4 more	GBenign/Likely benign
Select item 133607	NM_000051.4(ATM):c.2442C>A (p.Asp814Glu)	ATM (D814E)	Single nucleotide variant (missense variant)	not specified +6 more	GBenign
Select item 236691	NM_000051.4(ATM):c.2467-7C>T	ATM	Single nucleotide variant (intron variant)	Ataxia-telangiectasia syndrome +2 more	GConflicting classifications of pathogenicity
Select item 132736	NM_000051.4(ATM):c.2572T>C (p.Phe858Leu)	ATM (F858L)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +6 more	GBenign/Likely benign
Select item 127355	NM_000051.4(ATM):c.2608A>G (p.Asn870Asp)	ATM (N870D)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +5 more	GConflicting classifications of pathogenicity
Select item 133610	NM_000051.4(ATM):c.2614C>T (p.Pro872Ser)	ATM (P872S)	Single nucleotide variant (missense variant)	Familial cancer of breast	GBenign FDA Recognized database
Select item 140770	NM_000051.4(ATM):c.2685A>G (p.Leu895=)	ATM	Single nucleotide variant (synonymous variant)	Breast and/or ovarian cancer +6 more	GBenign
Select item 127358	NM_000051.4(ATM):c.2770C>T (p.Arg924Trp)	ATM (R924W)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +4 more	GUncertain significance
Select item 453436	NM_000051.4(ATM):c.2838+9C>A	ATM	Single nucleotide variant (intron variant)	not provided +2 more	GLikely benign
Select item 377508	NM_000051.4(ATM):c.2839-18T>C	ATM	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 141182	NM_000051.4(ATM):c.2921+1G>A	ATM	Single nucleotide variant (splice donor variant)	not specified +4 more	GPathogenic/Likely pathogenic
Select item 181855	NM_000051.4(ATM):c.2921+19dup	ATM	Duplication (intron variant)	not provided +5 more	GBenign/Likely benign
Select item 127362	NM_000051.4(ATM):c.2932T>C (p.Ser978Pro)	ATM (S978P)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 439418	NM_000051.4(ATM):c.3078-77C>T	ATM	Single nucleotide variant (intron variant)	not specified +3 more	GBenign
Select item 3027	NM_000051.4(ATM):c.3118A>G (p.Met1040Val)	ATM (M1040V)	Single nucleotide variant (missense variant)	Familial cancer of breast	GBenign FDA Recognized database
Select item 994202	NM_000051.4(ATM):c.3132T>C (p.Asn1044=)	ATM	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 132695	NM_000051.4(ATM):c.3161C>G (p.Pro1054Arg)	ATM (P1054R)	Single nucleotide variant (missense variant)	not specified +5 more	GBenign/Likely benign
Select item 234020	NM_000051.4(ATM):c.3256C>T (p.Arg1086Cys)	ATM (R1086C)	Single nucleotide variant (missense variant)	Familial cancer of breast +5 more	GConflicting classifications of pathogenicity
Select item 181941	NM_000051.4(ATM):c.3265G>T (p.Ala1089Ser)	ATM (A1089S)	Single nucleotide variant (missense variant)	not provided +5 more	GUncertain significance
Select item 181857	NM_000051.4(ATM):c.3285-9del	ATM	Deletion (intron variant)	not specified +4 more	GBenign/Likely benign
Select item 133615	NM_000051.4(ATM):c.3383A>G (p.Gln1128Arg)	ATM (Q1128R)	Single nucleotide variant (missense variant)	not specified +5 more	GBenign/Likely benign
Select item 181858	NM_000051.4(ATM):c.3403-13dup	ATM	Duplication (intron variant)	Ataxia-telangiectasia syndrome +4 more	GBenign/Likely benign
Select item 439422	NM_000051.3(ATM):c.3666A[5] (p.Asn1223Lysfs)	ATM (N1223fs)	Duplication (frameshift variant)	not specified	GPathogenic
Select item 127377	NM_000051.4(ATM):c.3925G>A (p.Ala1309Thr)	ATM (A1309T)	Single nucleotide variant (missense variant)	Familial cancer of breast	GBenign FDA Recognized database
Select item 136444	NM_000051.4(ATM):c.3993+5G>T	ATM	Single nucleotide variant (intron variant)	Breast and/or ovarian cancer +6 more	GBenign/Likely benign
Select item 132715	NM_000051.4(ATM):c.4042T>C (p.Leu1348=)	ATM	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +5 more	GBenign/Likely benign
Select item 127380	NM_000051.4(ATM):c.4066A>G (p.Asn1356Asp)	ATM (N1356D)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +4 more	GConflicting classifications of pathogenicity
Select item 236715	NM_000051.4(ATM):c.4091A>G (p.Asp1364Gly)	ATM (D1364G)	Single nucleotide variant (missense variant)	not specified +3 more	GUncertain significance
Select item 133619	NM_000051.4(ATM):c.4138C>T (p.His1380Tyr)	ATM (H1380Y)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +6 more	GBenign
Select item 181880	NM_000051.4(ATM):c.4143dup (p.Pro1382fs)	ATM (P1382fs)	Duplication (frameshift variant)	Ataxia-telangiectasia syndrome +3 more	GPathogenic
Select item 128456	NM_000051.4(ATM):c.4258C>T (p.Leu1420Phe)	ATM (L1420F)	Single nucleotide variant (missense variant)	not specified +5 more	GBenign/Likely benign
Select item 127385	NM_000051.4(ATM):c.4324T>C (p.Tyr1442His)	ATM (Y1442H)	Single nucleotide variant (missense variant)	not provided +7 more	GConflicting classifications of pathogenicity
Select item 127386	NM_000051.4(ATM):c.4362A>C (p.Lys1454Asn)	ATM (K1454N)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +4 more	GConflicting classifications of pathogenicity
Select item 127388	NM_000051.4(ATM):c.4388T>G (p.Phe1463Cys)	ATM (F1463C)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 127392	NM_000051.4(ATM):c.4424A>G (p.Tyr1475Cys)	ATM (Y1475C)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +6 more	GConflicting classifications of pathogenicity
Select item 1075345	NM_000051.4(ATM):c.4467del (p.Ser1490fs)	ATM (S1490fs)	Deletion (frameshift variant)	Ataxia-telangiectasia syndrome +1 more	GPathogenic
Select item 128457	NM_000051.4(ATM):c.4578C>T (p.Pro1526=)	ATM	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +5 more	GBenign/Likely benign
Select item 245791	NM_000051.4(ATM):c.4631A>G (p.Tyr1544Cys)	ATM (Y1544C)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +4 more	GUncertain significance
Select item 187337	NM_000051.4(ATM):c.4878T>C (p.Asp1626=)	ATM	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 490599	NM_000051.4(ATM):c.5005+17C>T	ATM	Single nucleotide variant (intron variant)	Ataxia-telangiectasia syndrome +2 more	GBenign/Likely benign
Select item 490600	NM_000051.4(ATM):c.5005+18G>A	ATM	Single nucleotide variant (intron variant)	Ataxia-telangiectasia syndrome +5 more	GBenign
Select item 127399	NM_000051.4(ATM):c.5071A>C (p.Ser1691Arg)	ATM (S1691R)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 439419	NM_000051.4(ATM):c.5357T>C (p.Phe1786Ser)	ATM (F1786S)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 127408	NM_000051.4(ATM):c.5489T>C (p.Met1830Thr)	ATM (M1830T)	Single nucleotide variant (missense variant)	Ataxia-telangiectasia syndrome +5 more	GUncertain significance
Select item 389165	NM_000051.4(ATM):c.5496+11T>C	ATM	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 136446	NM_000051.4(ATM):c.5497-15G>C	ATM	Single nucleotide variant (intron variant)	Breast and/or ovarian cancer +6 more	GConflicting classifications of pathogenicity
Select item 132706	NM_000051.4(ATM):c.5497-8T>C	ATM	Single nucleotide variant (intron variant)	Ataxia-telangiectasia syndrome +5 more	GBenign/Likely benign
Select item 128458	NM_000051.4(ATM):c.5557G>A (p.Asp1853Asn)	ATM (D1853N)	Single nucleotide variant (missense variant)	not specified +5 more	GBenign
Select item 133623	NM_000051.4(ATM):c.5558A>T (p.Asp1853Val)	ATM (D1853V)	Single nucleotide variant (missense variant)	not provided +6 more	GConflicting classifications of pathogenicity
Select item 489562	NM_000051.4(ATM):c.5675-13T>A	ATM	Single nucleotide variant (intron variant)	Ataxia-telangiectasia syndrome +2 more	GConflicting classifications of pathogenicity
Select item 482526	NM_000051.4(ATM):c.5692C>T (p.Arg1898Ter)	ATM (R1898*)	Single nucleotide variant (nonsense)	not provided +3 more	GPathogenic
Select item 128459	NM_000051.4(ATM):c.5793T>C (p.Ala1931=)	ATM, C11orf65	Single nucleotide variant (synonymous variant +1 more)	Ataxia-telangiectasia syndrome +6 more	GBenign/Likely benign
Select item 127412	NM_000051.4(ATM):c.5821G>C (p.Val1941Leu)	ATM, C11orf65 (V1941L)	Single nucleotide variant (missense variant +1 more)	not provided +5 more	GConflicting classifications of pathogenicity
Select item 133627	NM_000051.4(ATM):c.5948= (p.Ser1983=)	ATM, C11orf65	Single nucleotide variant (synonymous variant +2 more)	not provided +2 more	GBenign
Select item 127416	NM_000051.4(ATM):c.6067G>A (p.Gly2023Arg)	ATM, C11orf65 (G2023R)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +6 more	GConflicting classifications of pathogenicity
Select item 133628	NM_000051.4(ATM):c.6088A>G (p.Ile2030Val)	ATM, C11orf65 (I2030V)	Single nucleotide variant (missense variant +1 more)	not specified +6 more	GBenign/Likely benign
Select item 140766	NM_000051.4(ATM):c.6095+15T>C	ATM, C11orf65	Single nucleotide variant (intron variant)	Breast and/or ovarian cancer +6 more	GBenign
Select item 133629	NM_000051.4(ATM):c.6235G>A (p.Val2079Ile)	C11orf65, ATM (V2079I)	Single nucleotide variant (missense variant +1 more)	not specified +6 more	GBenign/Likely benign
Select item 181863	NM_000051.4(ATM):c.6348-8T>C	C11orf65, ATM	Single nucleotide variant (intron variant)	Ataxia-telangiectasia syndrome +3 more	GBenign/Likely benign
Select item 186642	NM_000051.4(ATM):c.6382T>C (p.Leu2128=)	ATM, C11orf65	Single nucleotide variant (synonymous variant +1 more)	ATM-related condition +4 more	GConflicting classifications of pathogenicity
Select item 218278	NM_000051.4(ATM):c.6415_6416del (p.Glu2139fs)	ATM, C11orf65 (E2139fs)	Microsatellite (frameshift variant +1 more)	not provided +4 more	GPathogenic

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