ClinVar Miner

List of variants in gene NOTCH2 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
NM_024408.4(NOTCH2):c.1248G>A (p.Val416=) rs374135765
NM_024408.4(NOTCH2):c.1677C>A (p.Ala559=) rs1553199554
NM_024408.4(NOTCH2):c.2226G>A (p.Lys742=) rs1570688503
NM_024408.4(NOTCH2):c.2295A>G (p.Pro765=) rs139358772
NM_024408.4(NOTCH2):c.2816C>T (p.Pro939Leu) rs201100122
NM_024408.4(NOTCH2):c.2830G>T (p.Asp944Tyr) rs151130105
NM_024408.4(NOTCH2):c.3075G>A (p.Glu1025=) rs782566942
NM_024408.4(NOTCH2):c.3222C>T (p.Asn1074=) rs1570674390
NM_024408.4(NOTCH2):c.3625T>G (p.Phe1209Val) rs147223770
NM_024408.4(NOTCH2):c.3913G>A (p.Val1305Ile) rs587688280
NM_024408.4(NOTCH2):c.4238T>A (p.Leu1413His) rs41313282
NM_024408.4(NOTCH2):c.4458G>A (p.Thr1486=) rs61756001
NM_024408.4(NOTCH2):c.6198T>C (p.Asn2066=) rs750891624
NM_024408.4(NOTCH2):c.6223G>A (p.Val2075Met) rs150516342
NM_024408.4(NOTCH2):c.660C>A (p.Ser220Arg) rs112650847

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.