ClinVar Miner

List of variants in gene ANK3 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_020987.5(ANK3):c.5137G>A (p.Val1713Ile) rs544357242 0.00134
NM_020987.5(ANK3):c.9935C>T (p.Ala3312Val) rs201625904 0.00101
NM_020987.5(ANK3):c.7469C>T (p.Pro2490Leu) rs140741466 0.00073
NM_020987.5(ANK3):c.4400A>G (p.Lys1467Arg) rs139982397 0.00056
NM_001204403.2(ANK3):c.86G>A (p.Ser29Asn) rs758576419 0.00019
NM_020987.5(ANK3):c.2555G>A (p.Arg852His) rs190358169 0.00014
NM_020987.5(ANK3):c.6982C>T (p.Arg2328Cys) rs147219129 0.00013
NM_020987.5(ANK3):c.13109A>T (p.His4370Leu) rs141713197 0.00010
NM_020987.5(ANK3):c.4504C>T (p.Pro1502Ser) rs142748584 0.00005
NM_020987.5(ANK3):c.10369C>T (p.Arg3457Cys) rs777814492 0.00004
NM_020987.5(ANK3):c.8674G>A (p.Asp2892Asn) rs769577208 0.00004
NM_020987.5(ANK3):c.1882G>A (p.Ala628Thr) rs540939855 0.00003
NM_020987.5(ANK3):c.5650C>A (p.Pro1884Thr) rs533377631 0.00003
NM_020987.5(ANK3):c.5939A>G (p.Asp1980Gly) rs1057523290 0.00003
NM_020987.5(ANK3):c.6695G>A (p.Arg2232Gln) rs770107349 0.00003
NM_020987.5(ANK3):c.6697G>T (p.Val2233Phe) rs748148709 0.00003
NM_020987.5(ANK3):c.10679G>A (p.Arg3560Gln) rs756241696 0.00002
NM_020987.5(ANK3):c.12520A>G (p.Ile4174Val) rs199850352 0.00002
NM_020987.5(ANK3):c.4052T>C (p.Val1351Ala) rs1057523750 0.00002
NM_020987.5(ANK3):c.11426C>T (p.Thr3809Ile) rs1057521542 0.00001
NM_020987.5(ANK3):c.12436G>A (p.Gly4146Arg) rs184370155 0.00001
NM_020987.5(ANK3):c.12656C>G (p.Thr4219Ser) rs745574366 0.00001
NM_020987.5(ANK3):c.1291G>A (p.Glu431Lys) rs1057523190 0.00001
NM_020987.5(ANK3):c.3917T>G (p.Ile1306Arg) rs754420265 0.00001
NM_020987.5(ANK3):c.4580C>A (p.Ser1527Tyr) rs765903434 0.00001
NM_020987.5(ANK3):c.6320C>G (p.Thr2107Ser) rs749819494 0.00001
NM_020987.5(ANK3):c.6667G>A (p.Ala2223Thr) rs761206620 0.00001
NM_020987.5(ANK3):c.7105G>T (p.Asp2369Tyr) rs759636712 0.00001
NM_020987.5(ANK3):c.7664T>C (p.Met2555Thr) rs146874315 0.00001
NM_020987.5(ANK3):c.7925C>G (p.Ser2642Cys) rs1057521794 0.00001
NM_020987.5(ANK3):c.10164C>G (p.Asn3388Lys) rs148635129
NM_020987.5(ANK3):c.1028A>C (p.Gln343Pro) rs1057521728
NM_020987.5(ANK3):c.10741G>A (p.Asp3581Asn) rs1057518261
NM_020987.5(ANK3):c.10867G>A (p.Asp3623Asn) rs368045259
NM_020987.5(ANK3):c.1162G>A (p.Asp388Asn) rs1057521304
NM_020987.5(ANK3):c.11927C>A (p.Thr3976Asn) rs765969303
NM_020987.5(ANK3):c.11990T>C (p.Ile3997Thr) rs370147674
NM_020987.5(ANK3):c.12098C>T (p.Ser4033Leu) rs1057523322
NM_020987.5(ANK3):c.12325G>T (p.Ala4109Ser) rs1554852167
NM_020987.5(ANK3):c.12596-1G>A rs1554844342
NM_020987.5(ANK3):c.12649A>G (p.Arg4217Gly)
NM_020987.5(ANK3):c.1436C>G (p.Ala479Gly) rs138255802
NM_020987.5(ANK3):c.1621C>T (p.Arg541Ter)
NM_020987.5(ANK3):c.1792G>A (p.Gly598Arg) rs770048872
NM_020987.5(ANK3):c.1870C>T (p.Pro624Ser)
NM_020987.5(ANK3):c.2143G>A (p.Val715Ile) rs1057524054
NM_020987.5(ANK3):c.2478+5G>A
NM_020987.5(ANK3):c.2677G>T (p.Gly893Cys)
NM_020987.5(ANK3):c.2746T>A (p.Ser916Thr) rs1057524507
NM_020987.5(ANK3):c.2949G>T (p.Gly983=)
NM_020987.5(ANK3):c.2984del (p.Gly995fs) rs1064796890
NM_020987.5(ANK3):c.3376A>G (p.Ile1126Val) rs1057524244
NM_020987.5(ANK3):c.3527G>A (p.Arg1176Gln) rs1057524303
NM_020987.5(ANK3):c.3575T>A (p.Ile1192Asn) rs747872965
NM_020987.5(ANK3):c.3581G>A (p.Gly1194Glu)
NM_020987.5(ANK3):c.4323G>C (p.Lys1441Asn) rs1057522936
NM_020987.5(ANK3):c.5408C>A (p.Ser1803Tyr) rs1057523766
NM_020987.5(ANK3):c.6017C>T (p.Ala2006Val)
NM_020987.5(ANK3):c.6508G>A (p.Val2170Ile)
NM_020987.5(ANK3):c.6937G>T (p.Ala2313Ser) rs949707021
NM_020987.5(ANK3):c.773C>T (p.Ala258Val)
NM_020987.5(ANK3):c.7963G>A (p.Asp2655Asn) rs1064796657
NM_020987.5(ANK3):c.8132_8133del (p.Lys2711fs) rs1064796891
NM_020987.5(ANK3):c.902G>A (p.Gly301Asp) rs1555147037
NM_020987.5(ANK3):c.9971A>G (p.Tyr3324Cys) rs1057522763

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