List of variants in gene KCNA1 reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000217.3(KCNA1):c.1440T>A (p.Thr480=)	rs4766309	0.75219
NM_000217.3(KCNA1):c.804G>C (p.Thr268=)	rs2227910	0.50318
NM_000217.3(KCNA1):c.*1681T>C	rs7974459	0.49866
NM_000217.3(KCNA1):c.*406C>T	rs4766311	0.48547
NM_000217.3(KCNA1):c.*3062T>C	rs10849174	0.47680
NM_000217.3(KCNA1):c.684T>C (p.Cys228=)	rs1048500	0.46819
NM_000217.3(KCNA1):c.*9G>A	rs4766310	0.45248
NM_000217.3(KCNA1):c.-110G>A	rs35678382	0.12116
NM_000217.3(KCNA1):c.*2174C>T	rs73050551	0.04497
NM_000217.3(KCNA1):c.*5141G>A	rs41482147	0.04492
NM_000217.3(KCNA1):c.*1524A>G	rs79357862	0.04290
NM_000217.3(KCNA1):c.-134G>T	rs12817318	0.03550
NM_000217.3(KCNA1):c.*786G>A	rs148607588	0.00564
NM_000217.3(KCNA1):c.1296C>G (p.Ser432=)	rs76066681	0.00299
NM_000217.3(KCNA1):c.237G>A (p.Glu79=)	rs149110871	0.00280
NM_000217.3(KCNA1):c.1327C>G (p.Arg443Gly)	rs150849316	0.00078
NM_000217.3(KCNA1):c.611G>A (p.Arg204His)	rs2229000	0.00063
NM_000217.3(KCNA1):c.114C>T (p.Arg38=)	rs146308797	0.00015
NM_000217.3(KCNA1):c.*5191G>A	rs575078827	0.00002
NM_000217.3(KCNA1):c.*2333G>A	rs2109420

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.