ClinVar Miner

List of variants in gene KCNA2 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004974.4(KCNA2):c.807C>T (p.Thr269=) rs146036196 0.00073
NM_004974.4(KCNA2):c.1047A>G (p.Ala349=) rs371979518 0.00026
NM_004974.4(KCNA2):c.372G>A (p.Glu124=) rs200499541 0.00026
NM_004974.4(KCNA2):c.30C>T (p.Asp10=) rs757960714 0.00007
NM_004974.4(KCNA2):c.972C>T (p.Ser324=) rs765820644 0.00004
NM_004974.4(KCNA2):c.*1209A>G rs1176245113 0.00001
NM_004974.4(KCNA2):c.1122T>C (p.Thr374=) rs373067199 0.00001
NM_004974.4(KCNA2):c.891G>T (p.Arg297=) rs538914802 0.00001
NM_004974.4(KCNA2):c.*1228G>C
NM_004974.4(KCNA2):c.1013G>A (p.Gly338Glu) rs1553181301
NM_004974.4(KCNA2):c.1184C>T (p.Ala395Val) rs1570752776
NM_004974.4(KCNA2):c.1208C>T (p.Ala403Val) rs1649457143
NM_004974.4(KCNA2):c.1214C>T (p.Pro405Leu)
NM_004974.4(KCNA2):c.1219C>G (p.Pro407Ala) rs1557731896
NM_004974.4(KCNA2):c.1250A>G (p.Tyr417Cys) rs1557731858
NM_004974.4(KCNA2):c.1255C>T (p.Arg419Trp) rs1421981152
NM_004974.4(KCNA2):c.238C>T (p.Arg80Trp) rs1448937059
NM_004974.4(KCNA2):c.345T>C (p.Phe115=)
NM_004974.4(KCNA2):c.393C>T (p.Gly131=) rs1649504612
NM_004974.4(KCNA2):c.440G>A (p.Arg147Lys)
NM_004974.4(KCNA2):c.512T>C (p.Met171Thr)
NM_004974.4(KCNA2):c.547G>A (p.Glu183Lys) rs1553181398
NM_004974.4(KCNA2):c.620A>G (p.Asn207Ser)
NM_004974.4(KCNA2):c.621C>A (p.Asn207Lys)
NM_004974.4(KCNA2):c.630C>T (p.Ile210=) rs761112803
NM_004974.4(KCNA2):c.881G>A (p.Arg294His) rs886041761
NM_004974.4(KCNA2):c.890G>A (p.Arg297Gln) rs786205232
NM_004974.4(KCNA2):c.894G>T (p.Leu298Phe) rs876657390

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.