ClinVar Miner

List of variants reported as benign for BENTA disease

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_032415.5(CARD11):c.1212G>A (p.Arg404=) rs142108678
NM_032415.5(CARD11):c.1260G>A (p.Glu420=) rs112171353
NM_032415.5(CARD11):c.1440G>A (p.Ser480=) rs41396348
NM_032415.5(CARD11):c.1590A>C (p.Glu530Asp) rs41515445
NM_032415.5(CARD11):c.1695C>T (p.Ala565=) rs41454944
NM_032415.5(CARD11):c.180G>T (p.Val60=) rs117016854
NM_032415.5(CARD11):c.225G>C (p.Arg75=) rs10229368
NM_032415.5(CARD11):c.2670G>A (p.Ser890=) rs146545469
NM_032415.5(CARD11):c.2748C>T (p.Asn916=) rs61731201
NM_032415.5(CARD11):c.2913C>T (p.Cys971=) rs61757651
NM_032415.5(CARD11):c.3019+6C>T rs199705831
NM_032415.5(CARD11):c.3019+7G>A rs184926618
NM_032415.5(CARD11):c.3019+9C>T rs200741645
NM_032415.5(CARD11):c.3090C>T (p.Asn1030=) rs112241277
NM_032415.5(CARD11):c.3144+9G>A rs112606562
NM_032415.5(CARD11):c.3399C>T (p.Arg1133=) rs117428786

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.