List of variants in gene KCNB1 reported as likely benign for not specified

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: 27

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004975.4(KCNB1):c.51G>A (p.Pro17=)	rs772184358	0.00022
NM_004975.4(KCNB1):c.-13G>A	rs1010817242	0.00019
NM_004975.4(KCNB1):c.1551G>A (p.Ser517=)	rs377030406	0.00014
NM_004975.4(KCNB1):c.*17G>A	rs368159173	0.00012
NM_004975.4(KCNB1):c.630G>A (p.Thr210=)	rs150723418	0.00011
NM_004975.4(KCNB1):c.1305T>C (p.Ala435=)	rs201403239	0.00009
NM_004975.4(KCNB1):c.-47G>A	rs569121895	0.00006
NM_004975.4(KCNB1):c.546C>T (p.Pro182=)	rs373223027	0.00006
NM_004975.4(KCNB1):c.2250G>A (p.Ala750=)	rs368736609	0.00005
NM_004975.4(KCNB1):c.504C>T (p.Cys168=)	rs139960830	0.00005
NM_004975.4(KCNB1):c.855C>T (p.Ser285=)	rs367938880	0.00005
NM_004975.4(KCNB1):c.1788A>T (p.Thr596=)	rs373119881	0.00002
NM_004975.4(KCNB1):c.2058C>T (p.Pro686=)	rs908785527	0.00002
NM_004975.4(KCNB1):c.2516C>T (p.Pro839Leu)	rs761070687	0.00002
NM_004975.4(KCNB1):c.568-20C>T	rs934317402	0.00002
NM_004975.4(KCNB1):c.568-9T>C	rs771401083	0.00002
NM_004975.4(KCNB1):c.96G>A (p.Arg32=)	rs781213174	0.00002
NM_004975.4(KCNB1):c.-29C>G	rs1044884348	0.00001
NM_004975.4(KCNB1):c.1116C>G (p.Thr372=)	rs1347667767	0.00001
NM_004975.4(KCNB1):c.2055C>A (p.Leu685=)	rs200849612	0.00001
NM_004975.4(KCNB1):c.411C>T (p.Tyr137=)	rs747090668	0.00001
NM_004975.4(KCNB1):c.711C>T (p.Ile237=)	rs1020438851	0.00001
NM_004975.4(KCNB1):c.81G>A (p.Lys27=)	rs910155179	0.00001
NM_004975.4(KCNB1):c.1570C>T (p.Leu524=)
NM_004975.4(KCNB1):c.1821C>T (p.Ser607=)	rs1057522569
NM_004975.4(KCNB1):c.813G>A (p.Leu271=)	rs763166574
NM_004975.4(KCNB1):c.939C>T (p.His313=)	rs1304387636

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.