ClinVar Miner

List of variants in gene ANK3 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP gnomAD frequency
NM_020987.5(ANK3):c.1047C>T (p.Cys349=) rs117138204 0.00580
NM_020987.5(ANK3):c.13106G>A (p.Arg4369Gln) rs141939315 0.00503
NM_020987.5(ANK3):c.7225T>C (p.Ser2409Pro) rs148904927 0.00459
NM_020987.5(ANK3):c.8508T>C (p.His2836=) rs11815168 0.00416
NM_020987.5(ANK3):c.2322G>C (p.Gly774=) rs138823660 0.00344
NM_020987.5(ANK3):c.10055A>G (p.Glu3352Gly) rs61845768 0.00329
NM_020987.5(ANK3):c.2889C>T (p.Tyr963=) rs149682716 0.00309
NM_020987.5(ANK3):c.5582C>T (p.Thr1861Met) rs117475706 0.00292
NM_020987.5(ANK3):c.2103C>T (p.Leu701=) rs142415903 0.00280
NM_020987.5(ANK3):c.756G>A (p.Thr252=) rs117266082 0.00280
NM_020987.5(ANK3):c.2674T>C (p.Leu892=) rs61732401 0.00273
NM_020987.5(ANK3):c.2316G>A (p.Gln772=) rs143430852 0.00240
NM_020987.5(ANK3):c.9997A>T (p.Thr3333Ser) rs140183285 0.00178
NM_020987.5(ANK3):c.10688A>G (p.Glu3563Gly) rs147527383 0.00177
NM_020987.5(ANK3):c.4465C>T (p.Pro1489Ser) rs41274676 0.00152
NM_020987.5(ANK3):c.1492-12C>A rs41283530 0.00138
NM_020987.5(ANK3):c.8534G>A (p.Gly2845Glu) rs139022925 0.00126
NM_020987.5(ANK3):c.11825A>G (p.Lys3942Arg) rs148549519 0.00116
NM_020987.5(ANK3):c.4029G>A (p.Glu1343=) rs116757606 0.00114
NM_020987.5(ANK3):c.3897G>A (p.Thr1299=) rs150367434 0.00106
NM_020987.5(ANK3):c.9935C>T (p.Ala3312Val) rs201625904 0.00101
NM_020987.5(ANK3):c.3822C>G (p.Ser1274=) rs184515022 0.00095
NM_020987.5(ANK3):c.399C>T (p.Val133=) rs77316697 0.00076
NM_020987.5(ANK3):c.4826C>T (p.Thr1609Met) rs148024054 0.00058
NM_020987.5(ANK3):c.6597T>G (p.Thr2199=) rs146801915 0.00056
NM_020987.5(ANK3):c.6555G>T (p.Gln2185His) rs144465058 0.00036
NM_020987.5(ANK3):c.2173G>A (p.Ala725Thr) rs144051466 0.00030
NM_020987.5(ANK3):c.11090C>G (p.Ser3697Cys) rs148109897 0.00024
NM_020987.5(ANK3):c.5981C>T (p.Ser1994Leu) rs141251507 0.00024
NM_020987.5(ANK3):c.2001C>T (p.Ser667=) rs146438080 0.00022
NM_020987.5(ANK3):c.4085G>C (p.Gly1362Ala) rs200556767 0.00019
NM_020987.5(ANK3):c.8512A>G (p.Thr2838Ala) rs200218631 0.00019
NM_020987.5(ANK3):c.3969C>T (p.Pro1323=) rs140104995 0.00017
NM_020987.5(ANK3):c.2385T>C (p.Asn795=) rs372094828 0.00014
NM_020987.5(ANK3):c.6945T>G (p.His2315Gln) rs375411220 0.00010
NM_020987.5(ANK3):c.9705C>T (p.Asp3235=) rs12769318 0.00008
NM_020987.5(ANK3):c.10020C>T (p.Asp3340=) rs750349884 0.00007
NM_020987.5(ANK3):c.11484A>G (p.Ser3828=) rs771625001 0.00007
NM_020987.5(ANK3):c.2976G>A (p.Ala992=) rs747475542 0.00006
NM_020987.5(ANK3):c.12108G>A (p.Thr4036=) rs763160108 0.00004
NM_020987.5(ANK3):c.8883C>T (p.Pro2961=) rs765123203 0.00002
NM_020987.5(ANK3):c.10749G>A (p.Thr3583=) rs985040592 0.00001
NM_020987.5(ANK3):c.12596-435G>A rs778947009 0.00001
NM_020987.5(ANK3):c.4530G>A (p.Pro1510=) rs757803121 0.00001
NM_020987.5(ANK3):c.8733C>G (p.Gly2911=) rs750979279 0.00001
NM_020987.5(ANK3):c.10164C>T (p.Asn3388=) rs148635129
NM_020987.5(ANK3):c.11476G>C (p.Val3826Leu)
NM_020987.5(ANK3):c.11826G>A (p.Lys3942=)
NM_020987.5(ANK3):c.12117C>T (p.Ser4039=)
NM_020987.5(ANK3):c.12294C>T (p.Ala4098=)
NM_020987.5(ANK3):c.12596-355G>T
NM_020987.5(ANK3):c.12672T>A (p.Asp4224Glu)
NM_020987.5(ANK3):c.1290C>G (p.Thr430=) rs374761322
NM_020987.5(ANK3):c.1419A>G (p.Ala473=)
NM_020987.5(ANK3):c.2086-7T>G
NM_020987.5(ANK3):c.2166T>C (p.His722=)
NM_020987.5(ANK3):c.2295G>A (p.Thr765=)
NM_020987.5(ANK3):c.273T>C (p.Ser91=)
NM_020987.5(ANK3):c.3105C>G (p.Pro1035=) rs55680239
NM_020987.5(ANK3):c.4608G>A (p.Pro1536=)
NM_020987.5(ANK3):c.4632G>A (p.Ser1544=)
NM_020987.5(ANK3):c.4662C>T (p.Gly1554=)
NM_020987.5(ANK3):c.5199T>C (p.Asn1733=)
NM_020987.5(ANK3):c.5331A>C (p.Pro1777=)
NM_020987.5(ANK3):c.5733C>T (p.Asp1911=)
NM_020987.5(ANK3):c.6684T>C (p.Asp2228=) rs2131980584
NM_020987.5(ANK3):c.6735C>T (p.His2245=)
NM_020987.5(ANK3):c.7449G>A (p.Ser2483=)
NM_020987.5(ANK3):c.8679A>G (p.Gln2893=)
NM_020987.5(ANK3):c.9145C>T (p.Pro3049Ser)

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