ClinVar Miner

List of variants in gene KCND3 reported by Athena Diagnostics Inc

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Gene type:
ClinVar version:
Total variants: 62
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HGVS dbSNP gnomAD frequency
NM_001378969.1(KCND3):c.669G>C (p.Ser223=) rs17215423 0.01872
NM_001378969.1(KCND3):c.375G>A (p.Pro125=) rs2289723 0.01862
NM_001378969.1(KCND3):c.1323C>T (p.Tyr441=) rs17215458 0.01243
NM_001378969.1(KCND3):c.1519-4G>T rs72548732 0.01109
NM_001378969.1(KCND3):c.957C>G (p.Ser319=) rs61733426 0.00386
NM_001378969.1(KCND3):c.1456A>G (p.Thr486Ala) rs149008060 0.00077
NM_001378969.1(KCND3):c.1573A>G (p.Met525Val) rs145890206 0.00076
NM_001378969.1(KCND3):c.5C>A (p.Ala2Glu) rs201340369 0.00066
NM_001378969.1(KCND3):c.1959C>T (p.Ser653=) rs147087785 0.00027
NM_001378969.1(KCND3):c.789C>T (p.Asp263=) rs373264592 0.00019
NM_001378969.1(KCND3):c.459G>A (p.Ser153=) rs755206508 0.00018
NM_001378969.1(KCND3):c.1106+10C>T rs377267051 0.00016
NM_001378969.1(KCND3):c.1292G>A (p.Arg431His) rs771703569 0.00015
NM_001378969.1(KCND3):c.696G>A (p.Ala232=) rs370453605 0.00014
NM_001378969.1(KCND3):c.1354G>A (p.Glu452Lys) rs200532657 0.00012
NM_001378969.1(KCND3):c.1062C>A (p.Ile354=) rs150934088 0.00009
NM_001378969.1(KCND3):c.207G>A (p.Thr69=) rs751347311 0.00009
NM_001378969.1(KCND3):c.1308C>G (p.Gly436=) rs190703406 0.00005
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.1314G>A (p.Ser438=) rs1247179970 0.00003
NM_001378969.1(KCND3):c.430G>A (p.Ala144Thr) rs143933558 0.00003
NM_001378969.1(KCND3):c.1794C>T (p.Asp598=) rs181971539 0.00002
NM_001378969.1(KCND3):c.321C>A (p.Arg107=) rs746952612 0.00002
NM_001378969.1(KCND3):c.1277G>A (p.Arg426His) rs760274429 0.00001
NM_001378969.1(KCND3):c.1427A>G (p.His476Arg) rs1571626155 0.00001
NM_001378969.1(KCND3):c.1697G>A (p.Arg566His) rs761867267 0.00001
NM_001378969.1(KCND3):c.553T>C (p.Phe185Leu) rs1219355757 0.00001
NM_001378969.1(KCND3):c.-1C>T rs2102000644
NM_001378969.1(KCND3):c.1027G>A (p.Glu343Lys) rs1557767012
NM_001378969.1(KCND3):c.1051T>C (p.Phe351Leu) rs1064794895
NM_001378969.1(KCND3):c.1054A>G (p.Thr352Ala) rs397515476
NM_001378969.1(KCND3):c.1094T>C (p.Met365Thr)
NM_001378969.1(KCND3):c.1109A>G (p.Tyr370Cys)
NM_001378969.1(KCND3):c.1130C>T (p.Thr377Met) rs1571636501
NM_001378969.1(KCND3):c.1150G>A (p.Gly384Ser) rs1664632655
NM_001378969.1(KCND3):c.1387G>A (p.Glu463Lys) rs1571626257
NM_001378969.1(KCND3):c.1411C>T (p.Leu471Phe) rs1064796735
NM_001378969.1(KCND3):c.1549G>C (p.Glu517Gln) rs202110939
NM_001378969.1(KCND3):c.1588T>A (p.Ser530Thr)
NM_001378969.1(KCND3):c.1696C>T (p.Arg566Cys)
NM_001378969.1(KCND3):c.1888C>T (p.Arg630Trp)
NM_001378969.1(KCND3):c.1920G>A (p.Thr640=)
NM_001378969.1(KCND3):c.228C>T (p.Asn76=) rs758608445
NM_001378969.1(KCND3):c.356C>A (p.Ala119Asp) rs2101998598
NM_001378969.1(KCND3):c.397T>C (p.Tyr133His) rs1553187539
NM_001378969.1(KCND3):c.407A>G (p.Tyr136Cys) rs1675000214
NM_001378969.1(KCND3):c.429C>T (p.Asn143=) rs1447033826
NM_001378969.1(KCND3):c.431C>T (p.Ala144Val)
NM_001378969.1(KCND3):c.433G>A (p.Glu145Lys) rs1557768261
NM_001378969.1(KCND3):c.446A>G (p.Asp149Gly) rs1217571134
NM_001378969.1(KCND3):c.44C>T (p.Ala15Val) rs866544148
NM_001378969.1(KCND3):c.492C>T (p.Ser164=) rs1170371506
NM_001378969.1(KCND3):c.633G>A (p.Pro211=) rs35131566
NM_001378969.1(KCND3):c.633G>T (p.Pro211=) rs35131566
NM_001378969.1(KCND3):c.667T>C (p.Ser223Pro) rs778053540
NM_001378969.1(KCND3):c.906C>G (p.Arg302=) rs575946174
NM_001378969.1(KCND3):c.91C>T (p.Pro31Ser) rs1403997481
NM_001378969.1(KCND3):c.937A>G (p.Thr313Ala) rs1553187267
NM_001378969.1(KCND3):c.957C>T (p.Ser319=) rs61733426
NM_001378969.1(KCND3):c.980C>T (p.Ser327Phe)

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