List of variants in gene SDHC reported as benign for not specified

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: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.77+32A>T	rs77828459	0.12254
NM_003001.5(SDHC):c.*123C>G	rs3813632	0.08037
NM_003001.5(SDHC):c.-32T>C	rs115782155	0.01342
NM_003001.5(SDHC):c.77+28A>T	rs199581931	0.01032
NM_003001.5(SDHC):c.*84G>C	rs201210474	0.00703
NM_003001.5(SDHC):c.78-23C>G	rs144938556	0.00658
NM_003001.5(SDHC):c.354T>C (p.Phe118=)	rs61733156	0.00454
NM_003001.5(SDHC):c.405+23C>T	rs373731336	0.00026
NM_003001.5(SDHC):c.120G>A (p.Arg40=)	rs36097930	0.00020
NM_003001.5(SDHC):c.342C>T (p.His114=)	rs143730978	0.00019
NM_003001.5(SDHC):c.179+10G>A	rs532455044	0.00006
NM_003001.5(SDHC):c.490A>T (p.Met164Leu)	rs200375156	0.00004
NM_003001.5(SDHC):c.406-14del	rs34744926
NM_003001.5(SDHC):c.406-14dup	rs34744926
NM_003001.5(SDHC):c.406-15_406-14del
NM_003001.5(SDHC):c.406-49A>G
NM_003001.5(SDHC):c.406-8G>T	rs747093483
NM_003001.5(SDHC):c.77+43del	rs368411074
NM_003001.5(SDHC):c.77+43dup	rs368411074

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.