ClinVar Miner

List of variants in gene CC2D2A reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_001378615.1(CC2D2A):c.1467-103G>A rs4698397 0.04920
NM_001378615.1(CC2D2A):c.2830-97A>G rs147979314 0.01803
NC_000004.12:g.15469808T>C rs28463577 0.01551
NM_001378615.1(CC2D2A):c.3015-295T>C rs75380803 0.01241
NM_001378615.1(CC2D2A):c.2004-214A>G rs16892138 0.01217
NM_001378615.1(CC2D2A):c.1149+253G>A rs183096710 0.01163
NM_001378615.1(CC2D2A):c.4675-169A>C rs6850488 0.01041
NM_001378615.1(CC2D2A):c.3772-39T>C rs28537702 0.01012
NM_001378615.1(CC2D2A):c.4314+130A>G rs558777331 0.00994
NM_001378615.1(CC2D2A):c.3014+281C>T rs138308149 0.00946
NM_001378615.1(CC2D2A):c.4496+142G>T rs114926503 0.00862
NM_001378615.1(CC2D2A):c.718-171C>T rs73799891 0.00750
NM_001378615.1(CC2D2A):c.438+261T>A rs568102516 0.00714
NM_001378615.1(CC2D2A):c.1150-158C>T rs141072393 0.00681
NM_001378615.1(CC2D2A):c.1149+255G>A rs560882066 0.00673
NM_001378615.1(CC2D2A):c.40-179A>C rs148503729 0.00640
NM_001378615.1(CC2D2A):c.4497-99T>C rs142321511 0.00623
NM_001378615.1(CC2D2A):c.4179+247G>A rs144446112 0.00622
NM_001378615.1(CC2D2A):c.4496+265T>A rs145908751 0.00608
NM_001378615.1(CC2D2A):c.2339-81G>C rs114741225 0.00590
NM_001378615.1(CC2D2A):c.4180-257T>C rs79847417 0.00553
NM_001378615.1(CC2D2A):c.1150-81G>A rs116497713 0.00552
NM_001378615.1(CC2D2A):c.1360-152A>G rs73798607 0.00510
NM_001378615.1(CC2D2A):c.2487-181T>C rs144857763 0.00508
NM_001378615.1(CC2D2A):c.3015-269G>A rs78227788 0.00507
NM_001378615.1(CC2D2A):c.4497-162G>A rs114612284 0.00497
NM_001378615.1(CC2D2A):c.439-28T>G rs148190483 0.00482
NM_001378615.1(CC2D2A):c.247+286T>G rs141540110 0.00480
NM_001378615.1(CC2D2A):c.4314+170G>A rs144270073 0.00466
NM_001378615.1(CC2D2A):c.1466+231C>T rs144943638 0.00416
NM_001378615.1(CC2D2A):c.4066-124G>A rs116581330 0.00416
NM_001378615.1(CC2D2A):c.3398+131C>T rs115284046 0.00403
NM_001378615.1(CC2D2A):c.4438-137T>C rs140464941 0.00394
NM_001378615.1(CC2D2A):c.1608-152T>C rs1558571 0.00365
NM_001378615.1(CC2D2A):c.247+259A>G rs114760230 0.00360
NM_001378615.1(CC2D2A):c.4065+229A>C rs540178152 0.00352
NM_001378615.1(CC2D2A):c.4496+163T>G rs142292638 0.00337
NM_001378615.1(CC2D2A):c.2625+204G>A rs141929992 0.00328
NM_001378615.1(CC2D2A):c.2626-260G>A rs78223914 0.00325
NM_001378615.1(CC2D2A):c.1359+26T>A rs10007035 0.00284
NM_001378615.1(CC2D2A):c.4459C>T (p.Arg1487Cys) rs186486235 0.00265
NM_001378615.1(CC2D2A):c.3288+25T>C rs73125629 0.00263
NM_001378615.1(CC2D2A):c.1607+265A>T rs185349028 0.00247
NM_001378615.1(CC2D2A):c.2487-11C>G rs374783761 0.00168
NM_001378615.1(CC2D2A):c.2050T>A (p.Leu684Ile) rs190698163 0.00159
NM_001378615.1(CC2D2A):c.2804G>A (p.Arg935Gln) rs187003641 0.00142
NM_001378615.1(CC2D2A):c.2181+7A>C rs143681243 0.00124
NM_001378615.1(CC2D2A):c.2813T>C (p.Met938Thr) rs61740537 0.00123
NM_001378615.1(CC2D2A):c.351T>G (p.Ser117Arg) rs186264635 0.00120
NM_001378615.1(CC2D2A):c.1162G>A (p.Val388Ile) rs115924432 0.00089
NM_001378615.1(CC2D2A):c.1956G>A (p.Pro652=) rs375131519 0.00080
NM_001378615.1(CC2D2A):c.355T>C (p.Leu119=) rs202150325 0.00059
NM_001378615.1(CC2D2A):c.1041C>T (p.Asp347=) rs371086728 0.00056
NM_001378615.1(CC2D2A):c.*1T>A rs199945435 0.00042
NM_001378615.1(CC2D2A):c.4438-31T>C rs147005127 0.00037
NM_001378615.1(CC2D2A):c.4296T>C (p.Cys1432=) rs372671421 0.00036
NM_001378615.1(CC2D2A):c.4438-9C>A rs117667651 0.00036
NM_001378615.1(CC2D2A):c.501G>T (p.Lys167Asn) rs190694237 0.00026
NM_001378615.1(CC2D2A):c.3480G>T (p.Leu1160=) rs771914973 0.00022
NM_001378615.1(CC2D2A):c.1731G>A (p.Ser577=) rs376746356 0.00014
NM_001378615.1(CC2D2A):c.1830G>A (p.Pro610=) rs185072004 0.00014
NM_001378615.1(CC2D2A):c.3014+4A>C rs748451478 0.00014
NM_001378615.1(CC2D2A):c.3744G>T (p.Leu1248=) rs755747140 0.00013
NM_001378615.1(CC2D2A):c.3872T>C (p.Ile1291Thr) rs370492044 0.00009
NM_001378615.1(CC2D2A):c.922T>C (p.Phe308Leu) rs201465430 0.00009
NM_001378615.1(CC2D2A):c.3381A>G (p.Glu1127=) rs373780145 0.00006
NM_001378615.1(CC2D2A):c.1116C>A (p.Ser372Arg) rs760839591 0.00004
NM_001378615.1(CC2D2A):c.2829+9C>T rs1009676697 0.00001
NM_001378615.1(CC2D2A):c.4326T>C (p.Asn1442=) rs780298185 0.00001
NM_001378615.1(CC2D2A):c.438+25T>G rs199546835 0.00001
NM_001378615.1(CC2D2A):c.1149+211dup rs397992357
NM_001378615.1(CC2D2A):c.123+132G>T rs146065951
NM_001378615.1(CC2D2A):c.123+654C>G rs111618236
NM_001378615.1(CC2D2A):c.1236G>A (p.Gly412=) rs1417156333
NM_001378615.1(CC2D2A):c.1978G>C (p.Val660Leu) rs16892134
NM_001378615.1(CC2D2A):c.2182-9_2182-8delinsAA rs1560177950
NM_001378615.1(CC2D2A):c.2486+143_2486+157del rs146708633
NM_001378615.1(CC2D2A):c.2728C>A (p.Arg910=) rs781206278
NM_001378615.1(CC2D2A):c.3145C>A (p.Arg1049=) rs386833750
NM_001378615.1(CC2D2A):c.336+120G>C rs142389729
NM_001378615.1(CC2D2A):c.3594+273_3594+304del rs368099911
NM_001378615.1(CC2D2A):c.4066-12del rs752759735
NM_001378615.1(CC2D2A):c.4314+126AT[4] rs1224228052
NM_001378615.1(CC2D2A):c.951G>A (p.Gly317=) rs762984980

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