ClinVar Miner

List of variants in gene ACTN2 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP
NM_001103.3(ACTN2):c.1089C>T (p.Ser363=) rs397516562
NM_001103.3(ACTN2):c.1108-247T>C
NM_001103.3(ACTN2):c.1255+95C>T
NM_001103.3(ACTN2):c.1287C>T (p.Tyr429=) rs764881077
NM_001103.3(ACTN2):c.1298C>T (p.Ser433Leu) rs143749154
NM_001103.3(ACTN2):c.1407-335A>G
NM_001103.3(ACTN2):c.1426G>A (p.Ala476Thr) rs142943120
NM_001103.3(ACTN2):c.1515+221T>A
NM_001103.3(ACTN2):c.1656+159G>A
NM_001103.3(ACTN2):c.1657-204G>A
NM_001103.3(ACTN2):c.1839+256T>C
NM_001103.3(ACTN2):c.1974+136C>T
NM_001103.3(ACTN2):c.1983C>T (p.Ala661=) rs372137571
NM_001103.3(ACTN2):c.2161C>A (p.Arg721Ser) rs149433837
NM_001103.3(ACTN2):c.2301+66G>T
NM_001103.3(ACTN2):c.2368-169C>A
NM_001103.3(ACTN2):c.536+223G>A
NM_001103.3(ACTN2):c.698-1009G>A
NM_001103.3(ACTN2):c.784-45A>G
NM_001103.3(ACTN2):c.784-525G>A

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.