ClinVar Miner

List of variants in gene ANK2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_001148.6(ANK2):c.4744C>T (p.Arg1582Trp) rs35249198 0.00403
NM_001148.6(ANK2):c.10395G>A (p.Glu3465=) rs147423696 0.00282
NM_001148.6(ANK2):c.1401A>G (p.Ala467=) rs142159132 0.00269
NM_001148.6(ANK2):c.4152T>C (p.Asp1384=) rs116128106 0.00267
NM_001148.6(ANK2):c.3543C>T (p.Ala1181=) rs76685232 0.00265
NM_001148.6(ANK2):c.3366C>T (p.Asn1122=) rs114896457 0.00256
NM_001148.6(ANK2):c.6648C>G (p.Gly2216=) rs140926982 0.00208
NM_001148.6(ANK2):c.10371G>A (p.Thr3457=) rs142908806 0.00203
NM_001148.6(ANK2):c.10901T>A (p.Val3634Asp) rs66785829 0.00200
NM_001148.6(ANK2):c.8354C>T (p.Ser2785Leu) rs145895389 0.00170
NM_001148.6(ANK2):c.10881T>G (p.His3627Gln) rs148405740 0.00029
NM_001148.6(ANK2):c.10531C>T (p.Leu3511=) rs148462839 0.00022
NM_001148.6(ANK2):c.3963T>C (p.Ile1321=) rs72901936 0.00020
NM_001148.6(ANK2):c.6633C>T (p.Ala2211=) rs143516811 0.00018
NM_001148.6(ANK2):c.270G>T (p.Val90=) rs376457094 0.00016
NM_001148.6(ANK2):c.2249A>G (p.Gln750Arg) rs371787039 0.00014
NM_001148.6(ANK2):c.2850C>A (p.Gly950=) rs189563238 0.00014
NM_001148.6(ANK2):c.4287A>G (p.Ser1429=) rs72556369 0.00011
NM_001148.6(ANK2):c.9690G>A (p.Thr3230=) rs755430079 0.00011
NM_001148.6(ANK2):c.11181C>T (p.Gly3727=) rs185569619 0.00009
NM_001148.6(ANK2):c.10032A>G (p.Pro3344=) rs775667097 0.00005
NM_001148.6(ANK2):c.9180A>G (p.Lys3060=) rs753698480 0.00005
NM_001148.6(ANK2):c.1773T>C (p.Ser591=) rs374775005 0.00004
NM_001148.6(ANK2):c.4653C>T (p.Ile1551=) rs200539502 0.00004
NM_001148.6(ANK2):c.11652A>G (p.Glu3884=) rs752145926 0.00002
NM_001148.6(ANK2):c.4777G>T (p.Val1593Phe) rs771802296 0.00002
NM_001148.6(ANK2):c.10674T>C (p.His3558=) rs761385520 0.00001
NM_001148.6(ANK2):c.11556C>T (p.Ala3852=) rs751064768 0.00001
NM_001148.6(ANK2):c.8768A>G (p.Gln2923Arg) rs551454026 0.00001
NM_001148.6(ANK2):c.11700T>C (p.Thr3900=)
NM_001148.6(ANK2):c.1863C>T (p.Ser621=)
NM_001148.6(ANK2):c.2736T>C (p.His912=)
NM_001148.6(ANK2):c.2900+5142C>T
NM_001148.6(ANK2):c.624C>T (p.Ala208=)
NM_001148.6(ANK2):c.6450C>T (p.Tyr2150=)
NM_001148.6(ANK2):c.8027G>C (p.Gly2676Ala)
NM_001148.6(ANK2):c.85-28511G>T
NM_001148.6(ANK2):c.85-28513C>T
NM_001148.6(ANK2):c.8586T>A (p.Asp2862Glu)

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