ClinVar Miner

List of variants in gene KCNT1 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 32
Download table as spreadsheet
HGVS dbSNP
NM_020822.2(KCNT1):c.1033C>A (p.Gln345Lys) rs1131691442
NM_020822.2(KCNT1):c.1067G>A (p.Arg356Gln) rs758152252
NM_020822.2(KCNT1):c.1077_1078delAG (p.Gly361Glnfs) rs796214553
NM_020822.2(KCNT1):c.1210G>A (p.Val404Met) rs368174673
NM_020822.2(KCNT1):c.1407C>G (p.His469Gln) rs537722828
NM_020822.2(KCNT1):c.1720delG (p.Glu574Serfs) rs1131691382
NM_020822.2(KCNT1):c.1726G>A (p.Glu576Lys) rs147306623
NM_020822.2(KCNT1):c.1840C>T (p.His614Tyr) rs1554775058
NM_020822.2(KCNT1):c.1898C>T (p.Ser633Leu) rs377750450
NM_020822.2(KCNT1):c.1975C>T (p.Arg659Cys) rs753599140
NM_020822.2(KCNT1):c.1996A>T (p.Ile666Phe) rs376231681
NM_020822.2(KCNT1):c.2048C>A (p.Pro683His) rs1411700632
NM_020822.2(KCNT1):c.2170_2184dup (p.Leu728_Ser729insProCysAspLeuLeu) rs757605635
NM_020822.2(KCNT1):c.2174G>C (p.Cys725Ser) rs756112023
NM_020822.2(KCNT1):c.218T>C (p.Leu73Pro) rs748537758
NM_020822.2(KCNT1):c.2244G>C (p.Glu748Asp) rs1333549995
NM_020822.2(KCNT1):c.2281G>A (p.Gly761Ser) rs761987610
NM_020822.2(KCNT1):c.2653A>G (p.Lys885Glu) rs974652934
NM_020822.2(KCNT1):c.2770_2771delCCinsG (p.Pro924Valfs) rs1554778336
NM_020822.2(KCNT1):c.3002C>A (p.Thr1001Lys) rs372775166
NM_020822.2(KCNT1):c.3197T>C (p.Val1066Ala) rs1554780631
NM_020822.2(KCNT1):c.3245G>A (p.Arg1082His) rs760151844
NM_020822.2(KCNT1):c.3317G>C (p.Arg1106Pro) rs561255614
NM_020822.2(KCNT1):c.3359C>T (p.Ala1120Val) rs745484103
NM_020822.2(KCNT1):c.3471G>A (p.Met1157Ile) rs1085307807
NM_020822.2(KCNT1):c.3563C>T (p.Thr1188Met) rs370090905
NM_020822.2(KCNT1):c.3584T>C (p.Ile1195Thr) rs777322392
NM_020822.2(KCNT1):c.3598C>T (p.Arg1200Cys) rs372028322
NM_020822.2(KCNT1):c.3689G>A (p.Arg1230His) rs776538404
NM_020822.2(KCNT1):c.3694G>A (p.Glu1232Lys) rs138109494
NM_020822.2(KCNT1):c.572C>G (p.Thr191Arg) rs1429039180
NM_020822.2(KCNT1):c.670A>G (p.Ile224Val) rs1554770959

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.