ClinVar Miner

List of variants in gene ANK3 reported as uncertain significance for Inborn genetic diseases

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Gene type:
ClinVar version:
Total variants: 128
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HGVS dbSNP gnomAD frequency
NM_020987.5(ANK3):c.6916A>G (p.Lys2306Glu) rs144270555 0.00022
NM_020987.5(ANK3):c.11497G>A (p.Gly3833Arg) rs191382767 0.00021
NM_020987.5(ANK3):c.8693T>C (p.Met2898Thr) rs150399982 0.00016
NM_020987.5(ANK3):c.9124G>A (p.Glu3042Lys) rs146205433 0.00014
NM_020987.5(ANK3):c.9160T>C (p.Phe3054Leu) rs138858281 0.00014
NM_020987.5(ANK3):c.3604A>G (p.Ile1202Val) rs138308296 0.00010
NM_020987.5(ANK3):c.104G>A (p.Arg35Gln) rs746466187 0.00006
NM_020987.5(ANK3):c.7501C>T (p.Arg2501Trp) rs759280618 0.00006
NM_020987.5(ANK3):c.3279T>A (p.Phe1093Leu) rs562083248 0.00005
NM_020987.5(ANK3):c.7672C>T (p.Arg2558Cys) rs375600068 0.00004
NM_020987.5(ANK3):c.11683T>C (p.Ser3895Pro) rs797045230 0.00003
NM_020987.5(ANK3):c.4601C>T (p.Ala1534Val) rs187577622 0.00003
NM_020987.5(ANK3):c.5933A>G (p.Lys1978Arg) rs201983331 0.00003
NM_020987.5(ANK3):c.8392G>A (p.Glu2798Lys) rs750733016 0.00003
NM_020987.5(ANK3):c.9706G>A (p.Val3236Met) rs747043475 0.00002
NM_020987.5(ANK3):c.10990G>A (p.Asp3664Asn) rs781254027 0.00001
NM_020987.5(ANK3):c.2126G>A (p.Arg709Gln) rs755310927 0.00001
NM_020987.5(ANK3):c.4070T>C (p.Ile1357Thr) rs765852674 0.00001
NM_020987.5(ANK3):c.4114A>C (p.Asn1372His) rs1379779681 0.00001
NM_020987.5(ANK3):c.7664T>C (p.Met2555Thr) rs146874315 0.00001
NM_020987.5(ANK3):c.7987G>A (p.Glu2663Lys) rs369092362 0.00001
NM_020987.5(ANK3):c.8054G>A (p.Ser2685Asn) rs750585326 0.00001
NM_020987.5(ANK3):c.9689G>A (p.Arg3230His) rs749129953 0.00001
NM_020987.5(ANK3):c.10000T>C (p.Phe3334Leu)
NM_020987.5(ANK3):c.10027C>G (p.Gln3343Glu)
NM_020987.5(ANK3):c.10103A>G (p.Asp3368Gly)
NM_020987.5(ANK3):c.10663T>G (p.Phe3555Val)
NM_020987.5(ANK3):c.10720C>T (p.Arg3574Cys)
NM_020987.5(ANK3):c.11114C>T (p.Ser3705Leu)
NM_020987.5(ANK3):c.11131A>G (p.Thr3711Ala)
NM_020987.5(ANK3):c.11255G>C (p.Cys3752Ser)
NM_020987.5(ANK3):c.11347A>G (p.Lys3783Glu)
NM_020987.5(ANK3):c.11526T>G (p.Asp3842Glu)
NM_020987.5(ANK3):c.11546A>G (p.Glu3849Gly)
NM_020987.5(ANK3):c.11581C>G (p.Gln3861Glu)
NM_020987.5(ANK3):c.11604G>T (p.Lys3868Asn)
NM_020987.5(ANK3):c.11711C>T (p.Ser3904Phe)
NM_020987.5(ANK3):c.11749A>G (p.Asn3917Asp)
NM_020987.5(ANK3):c.11762A>G (p.Asp3921Gly)
NM_020987.5(ANK3):c.11810A>G (p.Gln3937Arg)
NM_020987.5(ANK3):c.11911A>C (p.Thr3971Pro)
NM_020987.5(ANK3):c.11977T>C (p.Cys3993Arg)
NM_020987.5(ANK3):c.12029T>G (p.Leu4010Arg)
NM_020987.5(ANK3):c.12220G>A (p.Glu4074Lys)
NM_020987.5(ANK3):c.12637G>A (p.Ala4213Thr)
NM_020987.5(ANK3):c.12728G>A (p.Gly4243Glu)
NM_020987.5(ANK3):c.13037A>G (p.Glu4346Gly)
NM_020987.5(ANK3):c.13041G>C (p.Glu4347Asp)
NM_020987.5(ANK3):c.1745A>G (p.Asn582Ser)
NM_020987.5(ANK3):c.1795C>A (p.Leu599Ile)
NM_020987.5(ANK3):c.1994T>G (p.Ile665Ser)
NM_020987.5(ANK3):c.2026C>A (p.His676Asn)
NM_020987.5(ANK3):c.2067T>A (p.Asn689Lys)
NM_020987.5(ANK3):c.2269A>T (p.Asn757Tyr)
NM_020987.5(ANK3):c.2356A>G (p.Asn786Asp)
NM_020987.5(ANK3):c.2414G>A (p.Arg805His)
NM_020987.5(ANK3):c.2476A>T (p.Thr826Ser)
NM_020987.5(ANK3):c.2578C>T (p.Leu860Phe)
NM_020987.5(ANK3):c.2657C>T (p.Pro886Leu)
NM_020987.5(ANK3):c.3034C>T (p.Arg1012Cys)
NM_020987.5(ANK3):c.3062C>A (p.Thr1021Asn)
NM_020987.5(ANK3):c.3067C>T (p.Arg1023Cys)
NM_020987.5(ANK3):c.3091G>A (p.Ala1031Thr)
NM_020987.5(ANK3):c.3251A>T (p.Asn1084Ile)
NM_020987.5(ANK3):c.3410T>C (p.Val1137Ala)
NM_020987.5(ANK3):c.3556G>T (p.Asp1186Tyr)
NM_020987.5(ANK3):c.3709G>A (p.Asp1237Asn)
NM_020987.5(ANK3):c.3716C>T (p.Thr1239Ile)
NM_020987.5(ANK3):c.3943G>T (p.Val1315Phe)
NM_020987.5(ANK3):c.3967C>G (p.Pro1323Ala)
NM_020987.5(ANK3):c.4106G>C (p.Cys1369Ser)
NM_020987.5(ANK3):c.4381G>T (p.Ala1461Ser)
NM_020987.5(ANK3):c.4669A>C (p.Thr1557Pro)
NM_020987.5(ANK3):c.4729A>G (p.Met1577Val)
NM_020987.5(ANK3):c.4747A>T (p.Thr1583Ser)
NM_020987.5(ANK3):c.4853C>G (p.Ser1618Cys)
NM_020987.5(ANK3):c.5028G>C (p.Lys1676Asn)
NM_020987.5(ANK3):c.5128C>A (p.His1710Asn)
NM_020987.5(ANK3):c.5182T>C (p.Ser1728Pro)
NM_020987.5(ANK3):c.5201G>A (p.Gly1734Glu)
NM_020987.5(ANK3):c.5306C>T (p.Thr1769Ile)
NM_020987.5(ANK3):c.5443G>A (p.Val1815Ile) rs1589630328
NM_020987.5(ANK3):c.5536A>G (p.Thr1846Ala)
NM_020987.5(ANK3):c.5648C>G (p.Ala1883Gly)
NM_020987.5(ANK3):c.5695C>A (p.Gln1899Lys)
NM_020987.5(ANK3):c.5771C>T (p.Pro1924Leu)
NM_020987.5(ANK3):c.58G>C (p.Glu20Gln)
NM_020987.5(ANK3):c.6188G>A (p.Arg2063Lys)
NM_020987.5(ANK3):c.6208C>T (p.Pro2070Ser)
NM_020987.5(ANK3):c.6442G>A (p.Gly2148Ser)
NM_020987.5(ANK3):c.6541G>T (p.Gly2181Trp)
NM_020987.5(ANK3):c.6960C>A (p.Asn2320Lys)
NM_020987.5(ANK3):c.7049C>G (p.Thr2350Ser)
NM_020987.5(ANK3):c.7058A>G (p.His2353Arg)
NM_020987.5(ANK3):c.7099C>T (p.Arg2367Trp)
NM_020987.5(ANK3):c.7145C>T (p.Ala2382Val)
NM_020987.5(ANK3):c.7423G>A (p.Val2475Met)
NM_020987.5(ANK3):c.7502G>A (p.Arg2501Gln)
NM_020987.5(ANK3):c.7538A>G (p.Glu2513Gly)
NM_020987.5(ANK3):c.7736G>C (p.Arg2579Thr)
NM_020987.5(ANK3):c.781G>A (p.Val261Met)
NM_020987.5(ANK3):c.7913A>G (p.Glu2638Gly)
NM_020987.5(ANK3):c.7983G>C (p.Lys2661Asn)
NM_020987.5(ANK3):c.8177C>T (p.Thr2726Ile)
NM_020987.5(ANK3):c.8189G>C (p.Ser2730Thr)
NM_020987.5(ANK3):c.8269C>T (p.Pro2757Ser)
NM_020987.5(ANK3):c.8296A>G (p.Lys2766Glu)
NM_020987.5(ANK3):c.8323G>A (p.Asp2775Asn)
NM_020987.5(ANK3):c.8489C>A (p.Ala2830Asp)
NM_020987.5(ANK3):c.8527A>G (p.Thr2843Ala)
NM_020987.5(ANK3):c.8616T>G (p.His2872Gln)
NM_020987.5(ANK3):c.8659G>A (p.Glu2887Lys)
NM_020987.5(ANK3):c.8666A>G (p.Lys2889Arg)
NM_020987.5(ANK3):c.9084C>G (p.His3028Gln)
NM_020987.5(ANK3):c.9334G>C (p.Gly3112Arg)
NM_020987.5(ANK3):c.9388G>A (p.Gly3130Arg)
NM_020987.5(ANK3):c.9450T>G (p.Asp3150Glu)
NM_020987.5(ANK3):c.9706G>T (p.Val3236Leu)
NM_020987.5(ANK3):c.971C>G (p.Ala324Gly)
NM_020987.5(ANK3):c.971C>T (p.Ala324Val)
NM_020987.5(ANK3):c.9788A>T (p.Asp3263Val)
NM_020987.5(ANK3):c.9836T>A (p.Val3279Asp)
NM_020987.5(ANK3):c.9901A>G (p.Arg3301Gly)
NM_020987.5(ANK3):c.9926C>T (p.Pro3309Leu)
NM_020987.5(ANK3):c.9938A>T (p.Asp3313Val)
NM_020987.5(ANK3):c.9939C>A (p.Asp3313Glu) rs765015032
NM_020987.5(ANK3):c.9955G>A (p.Asp3319Asn)
NM_020987.5(ANK3):c.9968T>C (p.Ile3323Thr)

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