ClinVar Miner

List of variants in gene RAF1 reported as likely benign for canthal anomaly

Included ClinVar conditions (57):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
NM_001354689.3(RAF1):c.*160C>T rs5746246
NM_001354689.3(RAF1):c.*495C>T rs12808
NM_001354689.3(RAF1):c.*556G>A rs187286358
NM_001354689.3(RAF1):c.*606A>G rs556460176
NM_001354689.3(RAF1):c.-267G>A rs116247741
NM_001354689.3(RAF1):c.119G>A (p.Arg40His) rs192632236
NM_001354689.3(RAF1):c.1232G>T (p.Arg411Met) rs587782972
NM_001354689.3(RAF1):c.1689G>C (p.Thr563=) rs5746244
NM_001354689.3(RAF1):c.1815A>G (p.Val605=) rs3730296
NM_001354689.3(RAF1):c.1974G>A (p.Thr658=) rs144876026
NM_001354689.3(RAF1):c.2001C>T (p.Val667=) rs3730297
NM_001354689.3(RAF1):c.220A>G (p.Asn74Asp)
NM_001354689.3(RAF1):c.293T>C (p.Val98Ala) rs763559779
NM_001354689.3(RAF1):c.321-14T>A rs3730270
NM_001354689.3(RAF1):c.321-21dup rs202103447
NM_001354689.3(RAF1):c.505G>C (p.Gly169Arg) rs886039607
NM_001354689.3(RAF1):c.913A>G (p.Ser305Gly) rs150054973
NM_001354689.3(RAF1):c.983C>T (p.Pro328Leu) rs5746220
NM_002880.3(RAF1):c.-415-1C>G rs61730434

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.