ClinVar Miner

List of variants in gene ANK1 reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 118
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HGVS dbSNP gnomAD frequency
NM_000037.4(ANK1):c.2830G>A (p.Ala944Thr) rs35797405 0.00170
NM_000037.4(ANK1):c.4606C>T (p.Arg1536Cys) rs146416859 0.00121
NM_000037.4(ANK1):c.997G>A (p.Asp333Asn) rs147608206 0.00119
NM_000037.4(ANK1):c.1896G>A (p.Ser632=) rs140050236 0.00101
NM_000037.4(ANK1):c.3102C>T (p.Asn1034=) rs145169484 0.00101
NM_000037.4(ANK1):c.2960+13G>T rs200746947 0.00099
NM_000037.4(ANK1):c.690C>G (p.Ala230=) rs138331080 0.00098
NM_000037.4(ANK1):c.2132A>G (p.Tyr711Cys) rs139375455 0.00093
NM_000037.4(ANK1):c.1257C>T (p.Ile419=) rs139550171 0.00092
NM_000037.4(ANK1):c.2844C>T (p.Arg948=) rs7001141 0.00069
NM_000037.4(ANK1):c.4713G>A (p.Ala1571=) rs138394311 0.00068
NM_000037.4(ANK1):c.1483A>C (p.Asn495His) rs143839208 0.00057
NM_000037.4(ANK1):c.2796C>T (p.Asn932=) rs141257975 0.00054
NM_000037.4(ANK1):c.2167C>A (p.His723Asn) rs150899388 0.00039
NM_000037.4(ANK1):c.229-11A>G rs372152994 0.00035
NM_000037.4(ANK1):c.5395-1057C>T rs372282334 0.00034
NM_000037.4(ANK1):c.1194C>T (p.Asp398=) rs148471199 0.00030
NM_000037.4(ANK1):c.3984+9A>G rs369984591 0.00029
NM_000037.4(ANK1):c.876G>A (p.Leu292=) rs373060967 0.00026
NM_000037.4(ANK1):c.3533-10G>A rs374510116 0.00019
NM_000037.4(ANK1):c.4099G>A (p.Ala1367Thr) rs148620640 0.00019
NM_000037.4(ANK1):c.3282G>A (p.Thr1094=) rs144821829 0.00016
NM_000037.4(ANK1):c.3594C>T (p.Asn1198=) rs186020985 0.00016
NM_000037.4(ANK1):c.5376C>T (p.Thr1792=) rs147232364 0.00016
NM_000037.4(ANK1):c.5601G>A (p.Ala1867=) rs150975400 0.00016
NM_000037.4(ANK1):c.1293C>T (p.Asn431=) rs377436685 0.00014
NM_000037.4(ANK1):c.3045C>T (p.Ser1015=) rs112451551 0.00014
NM_000037.4(ANK1):c.4341T>C (p.Ser1447=) rs112677283 0.00014
NM_000037.4(ANK1):c.2982G>A (p.Pro994=) rs139623406 0.00013
NM_000037.4(ANK1):c.5574G>A (p.Pro1858=) rs139528300 0.00013
NM_000037.4(ANK1):c.3039C>T (p.Asn1013=) rs111620878 0.00012
NM_000037.4(ANK1):c.3288G>A (p.Pro1096=) rs140964621 0.00011
NM_000037.4(ANK1):c.3984+12C>T rs200019819 0.00011
NM_000037.4(ANK1):c.2389-10C>T rs764935260 0.00010
NM_000037.4(ANK1):c.1926C>T (p.Ala642=) rs534680895 0.00009
NM_000037.4(ANK1):c.4665G>A (p.Thr1555=) rs372732341 0.00009
NM_000037.4(ANK1):c.1859G>A (p.Ser620Asn) rs750068521 0.00008
NM_000037.4(ANK1):c.5124G>A (p.Ser1708=) rs143994699 0.00008
NM_000037.4(ANK1):c.1227C>T (p.His409=) rs572292527 0.00007
NM_000037.4(ANK1):c.1603-6C>T rs751217909 0.00007
NM_000037.4(ANK1):c.4105-5T>G rs768183148 0.00006
NM_000037.4(ANK1):c.5178G>A (p.Thr1726=) rs756122138 0.00006
NM_000037.4(ANK1):c.5223G>A (p.Gly1741=) rs145473653 0.00006
NM_000037.4(ANK1):c.624G>A (p.Thr208=) rs532040830 0.00006
NM_000037.4(ANK1):c.1801-18C>T rs756538201 0.00005
NM_000037.4(ANK1):c.4635C>T (p.Ala1545=) rs142386792 0.00004
NM_000037.4(ANK1):c.1341C>T (p.Ala447=) rs768336827 0.00003
NM_000037.4(ANK1):c.1563C>T (p.Ala521=) rs762615459 0.00002
NM_000037.4(ANK1):c.1968G>A (p.Ser656=) rs201462433 0.00002
NM_000037.4(ANK1):c.3115+8C>T rs747861245 0.00002
NM_000037.4(ANK1):c.3816G>A (p.Gln1272=) rs374155078 0.00002
NM_000037.4(ANK1):c.5395-1090G>A rs1291679242 0.00002
NM_000037.4(ANK1):c.5520C>T (p.Ala1840=) rs116148295 0.00002
NM_000037.4(ANK1):c.5544+59T>A rs770509350 0.00002
NM_000037.4(ANK1):c.723G>A (p.Thr241=) rs1170323588 0.00002
NM_000037.4(ANK1):c.117C>T (p.Asn39=) rs758866739 0.00001
NM_000037.4(ANK1):c.1578A>G (p.Glu526=) rs779446344 0.00001
NM_000037.4(ANK1):c.2424G>A (p.Glu808=) rs763085301 0.00001
NM_000037.4(ANK1):c.24C>T (p.Arg8=) rs764853398 0.00001
NM_000037.4(ANK1):c.3084C>T (p.Tyr1028=) rs1032459507 0.00001
NM_000037.4(ANK1):c.4023G>A (p.Ser1341=) rs371816885 0.00001
NM_000037.4(ANK1):c.4752T>G (p.Ser1584=) rs200897610 0.00001
NM_000037.4(ANK1):c.5232C>T (p.Pro1744=) rs146227434 0.00001
NM_000037.4(ANK1):c.5395-1080C>T rs143349452 0.00001
NM_000037.4(ANK1):c.711+13C>T rs763737257 0.00001
NM_000037.4(ANK1):c.882C>T (p.His294=) rs775318818 0.00001
NM_000037.4(ANK1):c.912C>T (p.Asn304=) rs377332629 0.00001
NM_000037.4(ANK1):c.96G>C (p.Leu32=) rs769077232 0.00001
NM_000037.4(ANK1):c.130-20C>T
NM_000037.4(ANK1):c.1359C>T (p.Ala453=) rs1586397519
NM_000037.4(ANK1):c.1383C>T (p.Ala461=)
NM_000037.4(ANK1):c.1602+12C>T
NM_000037.4(ANK1):c.1602+17C>T
NM_000037.4(ANK1):c.1660C>T (p.Leu554=)
NM_000037.4(ANK1):c.1695C>T (p.Ala565=)
NM_000037.4(ANK1):c.1890C>T (p.Ala630=)
NM_000037.4(ANK1):c.1944A>G (p.Ala648=)
NM_000037.4(ANK1):c.1998+18G>A
NM_000037.4(ANK1):c.1998+20A>T
NM_000037.4(ANK1):c.1999-18A>G rs2150616583
NM_000037.4(ANK1):c.2085C>T (p.Asp695=)
NM_000037.4(ANK1):c.2098-5T>C rs2150613009
NM_000037.4(ANK1):c.2196+12C>A
NM_000037.4(ANK1):c.219G>A (p.Thr73=) rs925701582
NM_000037.4(ANK1):c.2202A>G (p.Gly734=)
NM_000037.4(ANK1):c.2226C>G (p.Ala742=)
NM_000037.4(ANK1):c.2296-18G>T
NM_000037.4(ANK1):c.2520G>A (p.Glu840=) rs1182546869
NM_000037.4(ANK1):c.2558+15C>T
NM_000037.4(ANK1):c.2688C>G (p.Thr896=) rs377333429
NM_000037.4(ANK1):c.2691G>A (p.Glu897=)
NM_000037.4(ANK1):c.2799C>A (p.Gly933=) rs752186182
NM_000037.4(ANK1):c.28-17G>A
NM_000037.4(ANK1):c.2883G>A (p.Thr961=)
NM_000037.4(ANK1):c.2898C>T (p.Ala966=)
NM_000037.4(ANK1):c.2961-8T>C
NM_000037.4(ANK1):c.303A>T (p.Gly101=) rs1586511504
NM_000037.4(ANK1):c.318C>T (p.Ala106=)
NM_000037.4(ANK1):c.3228C>T (p.Ile1076=)
NM_000037.4(ANK1):c.327+10C>T rs1586510952
NM_000037.4(ANK1):c.3327+19G>T rs200871595
NM_000037.4(ANK1):c.3342G>A (p.Pro1114=) rs374102892
NM_000037.4(ANK1):c.3468C>T (p.Thr1156=) rs372816206
NM_000037.4(ANK1):c.3532+10G>A
NM_000037.4(ANK1):c.3532+20C>T
NM_000037.4(ANK1):c.3600C>T (p.Cys1200=)
NM_000037.4(ANK1):c.3615C>T (p.Thr1205=) rs1586144324
NM_000037.4(ANK1):c.3750C>T (p.Asp1250=) rs1273182651
NM_000037.4(ANK1):c.391C>T (p.Leu131=)
NM_000037.4(ANK1):c.4080C>T (p.Asn1360=)
NM_000037.4(ANK1):c.4098C>T (p.Cys1366=)
NM_000037.4(ANK1):c.4104+18G>A
NM_000037.4(ANK1):c.5145T>C (p.Asp1715=) rs1563357304
NM_000037.4(ANK1):c.5298C>T (p.Pro1766=)
NM_000037.4(ANK1):c.5395-1238T>G rs1585851432
NM_000037.4(ANK1):c.5526C>T (p.Ala1842=)
NM_000037.4(ANK1):c.5544+15G>T
NM_000037.4(ANK1):c.66A>G (p.Ser22=)

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