List of variants studied for benign neoplasm by CSER _CC_NCGL, University of Washington

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.*84G>C	rs201210474	0.00703
NM_017849.4(TMEM127):c.268G>A (p.Val90Met)	rs121908823	0.00264
NM_017849.4(TMEM127):c.217G>C (p.Gly73Arg)	rs121908820	0.00004
NM_003002.4(SDHD):c.158C>T (p.Pro53Leu)	rs149516118	0.00003
NM_003001.5(SDHC):c.8C>T (p.Ala3Val)	rs142139022	0.00001
NM_003000.3(SDHB):c.716C>G (p.Ser239Cys)	rs201098090
NM_003000.3(SDHB):c.79C>G (p.Arg27Gly)	rs74315369

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.