ClinVar Miner

List of variants reported as uncertain significance for Spinocerebellar ataxia type 19/22 by Invitae

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ClinVar version:
Total variants: 102
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HGVS dbSNP gnomAD frequency
NM_001378969.1(KCND3):c.641A>G (p.Lys214Arg) rs142744204 0.00034
NM_001378969.1(KCND3):c.1646G>A (p.Arg549His) rs35027371 0.00016
NM_001378969.1(KCND3):c.1703G>A (p.Arg568His) rs200212002 0.00007
NM_001378969.1(KCND3):c.1889G>A (p.Arg630Gln) rs774713377 0.00006
NM_001378969.1(KCND3):c.1769G>A (p.Arg590His) rs186194682 0.00005
NM_001378969.1(KCND3):c.1798G>A (p.Gly600Arg) rs149344567 0.00005
NM_001378969.1(KCND3):c.1649G>A (p.Arg550His) rs151164490 0.00004
NM_001378969.1(KCND3):c.1370C>T (p.Thr457Met) rs199637120 0.00003
NM_001378969.1(KCND3):c.1960G>A (p.Ala654Thr) rs774711788 0.00003
NM_001378969.1(KCND3):c.430G>A (p.Ala144Thr) rs143933558 0.00003
NM_001378969.1(KCND3):c.1502G>A (p.Arg501Gln) rs764928165 0.00002
NM_001378969.1(KCND3):c.1946T>C (p.Val649Ala) rs760907112 0.00002
NM_001378969.1(KCND3):c.514G>A (p.Ala172Thr) rs149488365 0.00002
NM_001378969.1(KCND3):c.1277G>A (p.Arg426His) rs760274429 0.00001
NM_001378969.1(KCND3):c.1313C>G (p.Ser438Trp) rs1172444288 0.00001
NM_001378969.1(KCND3):c.1393A>G (p.Met465Val) rs1245864814 0.00001
NM_001378969.1(KCND3):c.1427A>G (p.His476Arg) rs1571626155 0.00001
NM_001378969.1(KCND3):c.1478T>G (p.Val493Gly) rs1216457569 0.00001
NM_001378969.1(KCND3):c.1525G>A (p.Glu509Lys) rs760468985 0.00001
NM_001378969.1(KCND3):c.1634C>T (p.Thr545Ile) rs969494348 0.00001
NM_001378969.1(KCND3):c.1648C>T (p.Arg550Cys) rs778141653 0.00001
NM_001378969.1(KCND3):c.1697G>A (p.Arg566His) rs761867267 0.00001
NM_001378969.1(KCND3):c.1849A>G (p.Ile617Val) rs948125814 0.00001
NM_001378969.1(KCND3):c.1859C>A (p.Pro620His) rs758318696 0.00001
NM_001378969.1(KCND3):c.1861C>G (p.Pro621Ala) rs752495973 0.00001
NM_001378969.1(KCND3):c.1864G>T (p.Ala622Ser) rs1417756814 0.00001
NM_001378969.1(KCND3):c.1879G>A (p.Gly627Arg) rs372362132 0.00001
NM_001378969.1(KCND3):c.1943A>G (p.Asn648Ser) rs766562520 0.00001
NM_001378969.1(KCND3):c.346G>A (p.Asp116Asn) rs766584545 0.00001
NM_001378969.1(KCND3):c.622G>A (p.Gly208Ser) rs760097003 0.00001
NM_001378969.1(KCND3):c.739G>A (p.Ala247Thr) rs373756710 0.00001
NM_001378969.1(KCND3):c.89C>A (p.Ala30Asp) rs1307934269 0.00001
NM_001378969.1(KCND3):c.98A>T (p.Asp33Val) rs760460512 0.00001
NC_000001.10:g.(?_112524223)_(112525348_?)dup
NM_001378969.1(KCND3):c.1017G>A (p.Met339Ile) rs965641511
NM_001378969.1(KCND3):c.1040C>T (p.Ser347Leu)
NM_001378969.1(KCND3):c.1070C>G (p.Ser357Trp) rs867628133
NM_001378969.1(KCND3):c.110G>C (p.Arg37Pro) rs1675021542
NM_001378969.1(KCND3):c.1269+6C>T rs1060502174
NM_001378969.1(KCND3):c.1292G>C (p.Arg431Pro)
NM_001378969.1(KCND3):c.1292G>T (p.Arg431Leu) rs771703569
NM_001378969.1(KCND3):c.1336C>T (p.Arg446Cys) rs756087542
NM_001378969.1(KCND3):c.1339A>G (p.Asn447Asp) rs1571626928
NM_001378969.1(KCND3):c.1345C>T (p.Leu449Phe)
NM_001378969.1(KCND3):c.1351A>C (p.Asn451His)
NM_001378969.1(KCND3):c.1352A>G (p.Asn451Ser)
NM_001378969.1(KCND3):c.1369A>G (p.Thr457Ala)
NM_001378969.1(KCND3):c.1371+4G>C
NM_001378969.1(KCND3):c.1371+5G>T rs1178012198
NM_001378969.1(KCND3):c.1372G>A (p.Gly458Ser)
NM_001378969.1(KCND3):c.1384G>A (p.Glu462Lys)
NM_001378969.1(KCND3):c.1387G>A (p.Glu463Lys) rs1571626257
NM_001378969.1(KCND3):c.1406C>T (p.Thr469Ile)
NM_001378969.1(KCND3):c.1418A>T (p.Glu473Val) rs2101469294
NM_001378969.1(KCND3):c.1441C>A (p.His481Asn)
NM_001378969.1(KCND3):c.1496C>G (p.Ser499Cys) rs976664434
NM_001378969.1(KCND3):c.1518+4T>C rs1553235925
NM_001378969.1(KCND3):c.1535A>C (p.Asp512Ala) rs1664166577
NM_001378969.1(KCND3):c.1544T>C (p.Met515Thr)
NM_001378969.1(KCND3):c.1564G>A (p.Glu522Lys)
NM_001378969.1(KCND3):c.1574T>G (p.Met525Arg) rs1338355211
NM_001378969.1(KCND3):c.1600C>A (p.Pro534Thr) rs1447493103
NM_001378969.1(KCND3):c.1601C>T (p.Pro534Leu) rs1553235768
NM_001378969.1(KCND3):c.1672C>T (p.Pro558Ser) rs2101456436
NM_001378969.1(KCND3):c.1696C>T (p.Arg566Cys)
NM_001378969.1(KCND3):c.1709T>C (p.Met570Thr) rs1553235743
NM_001378969.1(KCND3):c.1715A>T (p.Glu572Val)
NM_001378969.1(KCND3):c.1741A>T (p.Ser581Cys) rs1420542041
NM_001378969.1(KCND3):c.1745A>G (p.Glu582Gly) rs2101456005
NM_001378969.1(KCND3):c.1754C>T (p.Ser585Phe)
NM_001378969.1(KCND3):c.1756C>G (p.Leu586Val) rs778053688
NM_001378969.1(KCND3):c.1772C>G (p.Ser591Cys) rs903701604
NM_001378969.1(KCND3):c.1784T>G (p.Leu595Trp) rs1483036958
NM_001378969.1(KCND3):c.1829T>C (p.Ile610Thr)
NM_001378969.1(KCND3):c.1856C>T (p.Thr619Ile)
NM_001378969.1(KCND3):c.1865C>A (p.Ala622Glu)
NM_001378969.1(KCND3):c.1873C>T (p.Pro625Ser) rs2101452061
NM_001378969.1(KCND3):c.1885A>T (p.Ser629Cys) rs1435444967
NM_001378969.1(KCND3):c.1895C>T (p.Pro632Leu) rs1261735013
NM_001378969.1(KCND3):c.1919C>T (p.Thr640Met)
NM_001378969.1(KCND3):c.1924A>T (p.Ile642Phe) rs754759010
NM_001378969.1(KCND3):c.1934T>C (p.Ile645Thr) rs1557929628
NM_001378969.1(KCND3):c.218T>A (p.Phe73Tyr)
NM_001378969.1(KCND3):c.256C>G (p.Arg86Gly) rs754042199
NM_001378969.1(KCND3):c.386G>C (p.Gly129Ala) rs1675001550
NM_001378969.1(KCND3):c.436C>T (p.Arg146Trp) rs575658111
NM_001378969.1(KCND3):c.446A>G (p.Asp149Gly) rs1217571134
NM_001378969.1(KCND3):c.448G>A (p.Asp150Asn) rs1488410733
NM_001378969.1(KCND3):c.478A>G (p.Met160Val) rs901416743
NM_001378969.1(KCND3):c.509G>T (p.Trp170Leu)
NM_001378969.1(KCND3):c.520G>C (p.Glu174Gln)
NM_001378969.1(KCND3):c.551T>C (p.Val184Ala) rs2101997398
NM_001378969.1(KCND3):c.566C>G (p.Thr189Ser)
NM_001378969.1(KCND3):c.668C>T (p.Ser223Leu)
NM_001378969.1(KCND3):c.685C>G (p.Leu229Val)
NM_001378969.1(KCND3):c.715G>C (p.Val239Leu) rs2101996463
NM_001378969.1(KCND3):c.739G>T (p.Ala247Ser)
NM_001378969.1(KCND3):c.82C>A (p.Pro28Thr) rs1675024873
NM_001378969.1(KCND3):c.878G>A (p.Arg293His) rs1674965278
NM_001378969.1(KCND3):c.917G>A (p.Gly306Asp) rs2101995501
NM_001378969.1(KCND3):c.91C>T (p.Pro31Ser) rs1403997481
NM_001378969.1(KCND3):c.930G>A (p.Leu310=) rs577883061

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