ClinVar Miner

List of variants in gene NOTCH2 reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP
NM_024408.4(NOTCH2):c.1315G>A (p.Ala439Thr) rs199565938
NM_024408.4(NOTCH2):c.3034T>C (p.Leu1012=) rs77194332
NM_024408.4(NOTCH2):c.3117G>A (p.Thr1039=) rs36084504
NM_024408.4(NOTCH2):c.3234C>T (p.Cys1078=) rs7543643
NM_024408.4(NOTCH2):c.3441G>A (p.Glu1147=) rs371875533
NM_024408.4(NOTCH2):c.3479A>G (p.His1160Arg) rs142876168
NM_024408.4(NOTCH2):c.3519C>T (p.Cys1173=) rs115325955
NM_024408.4(NOTCH2):c.3625T>G (p.Phe1209Val) rs147223770
NM_024408.4(NOTCH2):c.3779G>A (p.Arg1260His) rs75423398
NM_024408.4(NOTCH2):c.3980A>G (p.Asp1327Gly) rs61752484
NM_024408.4(NOTCH2):c.4014C>T (p.Ser1338=) rs17024525
NM_024408.4(NOTCH2):c.4238T>A (p.Leu1413His) rs41313282
NM_024408.4(NOTCH2):c.4305G>A (p.Arg1435=) rs6692009
NM_024408.4(NOTCH2):c.4311C>T (p.Gly1437=) rs34561092
NM_024408.4(NOTCH2):c.5065A>T (p.Ile1689Phe) rs60854092
NM_024408.4(NOTCH2):c.6421C>T (p.Leu2141=) rs3795666
NM_024408.4(NOTCH2):c.7075C>G (p.Pro2359Ala) rs75831573
NM_024408.4(NOTCH2):c.939C>T (p.Gly313=) rs7533978

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.