List of variants in gene SDHC reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.*84G>C	rs201210474	0.00703
NM_003001.5(SDHC):c.354T>C (p.Phe118=)	rs61733156	0.00454
NM_003001.5(SDHC):c.*78G>A	rs182629842	0.00182
NM_003001.4(SDHC):c.*1159C>T	rs760243208	0.00180
NM_003001.5(SDHC):c.120G>A (p.Arg40=)	rs36097930	0.00020
NM_003001.5(SDHC):c.490A>T (p.Met164Leu)	rs200375156	0.00004
NM_003001.5(SDHC):c.99G>A (p.Thr33=)	rs145535502	0.00003
NM_003001.5(SDHC):c.148C>T (p.Arg50Cys)	rs587778661	0.00001
NM_003001.5(SDHC):c.397C>T (p.Arg133Ter)	rs764575966	0.00001
NM_003001.5(SDHC):c.405+1G>T	rs587776653	0.00001
NM_003001.5(SDHC):c.8C>T (p.Ala3Val)	rs142139022	0.00001
NM_003001.5(SDHC):c.21-2A>G	rs1131691062
NM_003001.5(SDHC):c.294T>G (p.Ser98=)	rs376292127

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