ClinVar Miner

List of variants in gene ATM reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 78
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HGVS dbSNP
NC_000011.10:g.108279640_108279642del
NM_000051.3(ATM):c.-14T>C
NM_000051.3(ATM):c.-18G>A rs374303671
NM_000051.3(ATM):c.-30-180C>T
NM_000051.3(ATM):c.1020C>T (p.Ala340=) rs546927781
NM_000051.3(ATM):c.103C>A (p.Arg35=) rs55861249
NM_000051.3(ATM):c.1229T>C (p.Val410Ala) rs56128736
NM_000051.3(ATM):c.1236-193C>T
NM_000051.3(ATM):c.1272T>C (p.Pro424=) rs35578748
NM_000051.3(ATM):c.1314A>C (p.Ile438=) rs770573462
NM_000051.3(ATM):c.1368A>G (p.Leu456=) rs750579940
NM_000051.3(ATM):c.1380G>C (p.Thr460=) rs145333518
NM_000051.3(ATM):c.146C>G (p.Ser49Cys) rs1800054
NM_000051.3(ATM):c.1595G>A (p.Cys532Tyr) rs35963548
NM_000051.3(ATM):c.162T>C (p.Tyr54=) rs3218690
NM_000051.3(ATM):c.1744T>C (p.Phe582Leu) rs2235006
NM_000051.3(ATM):c.1779A>G (p.Thr593=) rs876660493
NM_000051.3(ATM):c.1803-154G>A
NM_000051.3(ATM):c.185+16T>C rs1343329254
NM_000051.3(ATM):c.1953A>G (p.Leu651=) rs730881283
NM_000051.3(ATM):c.1986T>C (p.Phe662=) rs1800055
NM_000051.3(ATM):c.201T>C (p.Tyr67=) rs1555055083
NM_000051.3(ATM):c.2289T>A (p.Phe763Leu) rs34231402
NM_000051.3(ATM):c.2403C>A (p.Gly801=)
NM_000051.3(ATM):c.2522A>C (p.Asp841Ala) rs587781812
NM_000051.3(ATM):c.2532A>G (p.Gly844=) rs755261743
NM_000051.3(ATM):c.2805G>C (p.Thr935=) rs55934812
NM_000051.3(ATM):c.2839-337G>A
NM_000051.3(ATM):c.2839-384T>A
NM_000051.3(ATM):c.2917C>T (p.Leu973=) rs535646511
NM_000051.3(ATM):c.2932T>C (p.Ser978Pro) rs139552233
NM_000051.3(ATM):c.3012C>T (p.Ser1004=) rs751260996
NM_000051.3(ATM):c.3077+209C>G
NM_000051.3(ATM):c.3118A>G (p.Met1040Val) rs3092857
NM_000051.3(ATM):c.3273G>A (p.Glu1091=) rs762860946
NM_000051.3(ATM):c.332-158T>A
NM_000051.3(ATM):c.3324G>C (p.Leu1108=) rs762269034
NM_000051.3(ATM):c.3342G>A (p.Lys1114=) rs138393322
NM_000051.3(ATM):c.3383A>G (p.Gln1128Arg) rs2229020
NM_000051.3(ATM):c.3402+70A>G
NM_000051.3(ATM):c.3403-14_3403-13dupAA
NM_000051.3(ATM):c.370A>G (p.Ile124Val) rs148590073
NM_000051.3(ATM):c.3746+4A>G
NM_000051.3(ATM):c.3925G>A (p.Ala1309Thr) rs149711770
NM_000051.3(ATM):c.3993+40G>A
NM_000051.3(ATM):c.3993+5G>T rs3092842
NM_000051.3(ATM):c.3994-111C>G
NM_000051.3(ATM):c.3994-121delC rs56013141
NM_000051.3(ATM):c.3994-50C>T
NM_000051.3(ATM):c.4071T>C (p.Ser1357=) rs767516955
NM_000051.3(ATM):c.4109+6T>C rs368606937
NM_000051.3(ATM):c.4377A>C (p.Gly1459=) rs1565456710
NM_000051.3(ATM):c.4388T>G (p.Phe1463Cys) rs138327406
NM_000051.3(ATM):c.4424A>G (p.Tyr1475Cys) rs34640941
NM_000051.3(ATM):c.4473C>T (p.Phe1491=) rs4988008
NM_000051.3(ATM):c.4482T>C (p.Cys1494=) rs769071554
NM_000051.3(ATM):c.4626G>A (p.Leu1542=) rs786202784
NM_000051.3(ATM):c.4779A>G (p.Glu1593=) rs587778076
NM_000051.3(ATM):c.4878T>C (p.Asp1626=) rs755687834
NM_000051.3(ATM):c.493T>C (p.Leu165=) rs878853514
NM_000051.3(ATM):c.4949A>G (p.Asn1650Ser) rs55870064
NM_000051.3(ATM):c.496+18T>C rs762171014
NM_000051.3(ATM):c.496+20G>C rs751245102
NM_000051.3(ATM):c.4980C>T (p.Asn1660=) rs144338238
NM_000051.3(ATM):c.5071A>C (p.Ser1691Arg) rs1800059
NM_000051.3(ATM):c.5178-150T>C
NM_000051.3(ATM):c.5320-171C>A
NM_000051.3(ATM):c.5320-74T>C
NM_000051.3(ATM):c.5497-168T>C
NM_000051.3(ATM):c.5674+102A>G
NM_000051.3(ATM):c.5675-4T>A rs56075338
NM_000051.3(ATM):c.5762+119G>A
NM_000051.3(ATM):c.609C>T (p.Asp203=) rs144709948
NM_000051.3(ATM):c.901+99C>A
NM_000051.3(ATM):c.975T>C (p.His325=) rs746825207
NM_000051.3(ATM):c.998C>T (p.Ser333Phe) rs28904919
NM_000051.3:c.4237-8T>C
NM_000051.3:c.5319+3C>A

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