List of variants in gene NSDHL reported as pathogenic for benign neoplasm

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_015922.3(NSDHL):c.1038_1041dup (p.Gly348fs)	rs797045835
NM_015922.3(NSDHL):c.262C>T (p.Arg88Ter)	rs104894903
NM_015922.3(NSDHL):c.314C>T (p.Ala105Val)	rs104894909
NM_015922.3(NSDHL):c.451G>T (p.Glu151Ter)	rs104894905
NM_015922.3(NSDHL):c.544G>C (p.Ala182Pro)	rs104894904
NM_015922.3(NSDHL):c.613G>A (p.Gly205Ser)	rs104894901
NM_015922.3(NSDHL):c.628C>T (p.Gln210Ter)	rs104894902
NM_015922.3(NSDHL):c.757C>T (p.Gln253Ter)	rs141571609
NM_015922.3(NSDHL):c.904del (p.Tyr302fs)	rs587784225
NM_015922.3(NSDHL):c.906C>A (p.Tyr302Ter)	rs587784226

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.