ClinVar Miner

List of variants in gene ANK3 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_020987.5(ANK3):c.11366A>G (p.Asn3789Ser) rs144123544 0.00043
NM_020987.5(ANK3):c.8573C>T (p.Ser2858Leu) rs78194762 0.00023
NM_020987.5(ANK3):c.6916A>G (p.Lys2306Glu) rs144270555 0.00022
NM_020987.5(ANK3):c.11159C>T (p.Thr3720Met) rs201547988 0.00014
NM_020987.5(ANK3):c.4868G>A (p.Arg1623Gln) rs143606308 0.00009
NM_020987.5(ANK3):c.10397T>A (p.Val3466Asp) rs201398340 0.00007
NM_020987.5(ANK3):c.671A>G (p.Asn224Ser) rs200837964 0.00006
NM_020987.5(ANK3):c.3279T>A (p.Phe1093Leu) rs562083248 0.00005
NM_020987.5(ANK3):c.10369C>T (p.Arg3457Cys) rs777814492 0.00004
NM_020987.5(ANK3):c.6661A>G (p.Met2221Val) rs765007870 0.00004
NM_020987.5(ANK3):c.7487A>C (p.Gln2496Pro) rs368439840 0.00004
NM_020987.5(ANK3):c.8589T>G (p.Asn2863Lys) rs149138713 0.00004
NM_020987.5(ANK3):c.10990G>A (p.Asp3664Asn) rs781254027 0.00001
NM_020987.5(ANK3):c.12079G>A (p.Asp4027Asn) rs561525408 0.00001
NM_020987.5(ANK3):c.12368G>A (p.Arg4123His) rs780088040 0.00001
NM_020987.5(ANK3):c.12767_12769del (p.Glu4256_Ile4257delinsVal) rs1425594215 0.00001
NM_020987.5(ANK3):c.7987G>A (p.Glu2663Lys) rs369092362 0.00001
NM_020987.5(ANK3):c.8048A>C (p.Glu2683Ala) rs775797548 0.00001
NM_020987.5(ANK3):c.8684A>G (p.Asn2895Ser) rs747994876 0.00001
NM_020987.5(ANK3):c.9962A>G (p.Glu3321Gly) rs140902380 0.00001
NM_020987.5(ANK3):c.10019A>T (p.Asp3340Val) rs1337459791
NM_020987.5(ANK3):c.10717G>T (p.Asp3573Tyr)
NM_020987.5(ANK3):c.11007C>A (p.Thr3669=) rs2131966858
NM_020987.5(ANK3):c.11068G>A (p.Gly3690Arg)
NM_020987.5(ANK3):c.11111A>C (p.Lys3704Thr)
NM_020987.5(ANK3):c.11156G>A (p.Arg3719His)
NM_020987.5(ANK3):c.11804A>G (p.Gln3935Arg)
NM_020987.5(ANK3):c.11898CAC[6] (p.Thr3978dup) rs548780827
NM_020987.5(ANK3):c.11950G>A (p.Val3984Ile)
NM_020987.5(ANK3):c.11977T>C (p.Cys3993Arg)
NM_020987.5(ANK3):c.12227G>A (p.Arg4076Lys)
NM_020987.5(ANK3):c.12587C>T (p.Pro4196Leu)
NM_020987.5(ANK3):c.12596-306T>A
NM_020987.5(ANK3):c.13082A>T (p.Lys4361Met) rs2076325400
NM_020987.5(ANK3):c.1340A>T (p.Asn447Ile) rs1565651946
NM_020987.5(ANK3):c.1491+1G>A
NM_020987.5(ANK3):c.1681A>G (p.Thr561Ala)
NM_020987.5(ANK3):c.2047C>T (p.Leu683Phe)
NM_020987.5(ANK3):c.2164C>T (p.His722Tyr) rs267602541
NM_020987.5(ANK3):c.2743C>T (p.Arg915Cys)
NM_020987.5(ANK3):c.2837A>C (p.Glu946Ala) rs1347320438
NM_020987.5(ANK3):c.287G>A (p.Arg96Lys) rs1592956332
NM_020987.5(ANK3):c.3199T>G (p.Phe1067Val)
NM_020987.5(ANK3):c.3218A>G (p.Lys1073Arg) rs2092116910
NM_020987.5(ANK3):c.3962A>G (p.Asn1321Ser)
NM_020987.5(ANK3):c.4336G>C (p.Asp1446His) rs1589722025
NM_020987.5(ANK3):c.5077A>C (p.Lys1693Gln)
NM_020987.5(ANK3):c.5443G>A (p.Val1815Ile) rs1589630328
NM_020987.5(ANK3):c.5519C>T (p.Pro1840Leu) rs770723563
NM_020987.5(ANK3):c.652G>A (p.Ala218Thr)
NM_020987.5(ANK3):c.7000A>G (p.Ile2334Val)
NM_020987.5(ANK3):c.7100G>A (p.Arg2367Gln)
NM_020987.5(ANK3):c.7669A>T (p.Met2557Leu)
NM_020987.5(ANK3):c.7909A>T (p.Thr2637Ser)
NM_020987.5(ANK3):c.7983G>C (p.Lys2661Asn)
NM_020987.5(ANK3):c.8199G>A (p.Met2733Ile)
NM_020987.5(ANK3):c.8458G>C (p.Ala2820Pro) rs1452344286
NM_020987.5(ANK3):c.8773T>G (p.Ser2925Ala)
NM_020987.5(ANK3):c.9328CAA[1] (p.Gln3111del)
NM_020987.5(ANK3):c.98G>A (p.Arg33Gln)

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