List of variants in gene SDHC reported as uncertain significance by Quest Diagnostics Nichols Institute San Juan Capistrano

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

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HGVS	dbSNP	gnomAD frequency
NM_003001.5(SDHC):c.98C>T (p.Thr33Met)	rs148566767	0.00007
NM_003001.5(SDHC):c.119G>A (p.Arg40Gln)	rs772450693	0.00005
NM_003001.5(SDHC):c.118C>T (p.Arg40Trp)	rs978019587	0.00004
NM_003001.5(SDHC):c.490A>T (p.Met164Leu)	rs200375156	0.00004
NM_003001.5(SDHC):c.292T>G (p.Ser98Ala)	rs371462564	0.00002
NM_003001.5(SDHC):c.11T>C (p.Leu4Pro)	rs774299337	0.00001
NM_003001.5(SDHC):c.15G>T (p.Leu5Phe)	rs771746264	0.00001
NM_003001.5(SDHC):c.295T>C (p.Tyr99His)	rs760678574	0.00001
NM_003001.5(SDHC):c.40C>T (p.Leu14Phe)	rs760986608	0.00001
NM_003001.5(SDHC):c.431A>C (p.Lys144Thr)	rs876659889	0.00001
NM_003001.5(SDHC):c.127A>C (p.Asn43His)	rs1553262439
NM_003001.5(SDHC):c.13T>A (p.Leu5Met)	rs894925936
NM_003001.5(SDHC):c.165C>T (p.His55=)	rs786202080
NM_003001.5(SDHC):c.183G>C (p.Trp61Cys)	rs1571869120
NM_003001.5(SDHC):c.232T>G (p.Leu78Val)	rs1553264225
NM_003001.5(SDHC):c.351G>A (p.Lys117=)	rs1571890344
NM_003001.5(SDHC):c.363C>T (p.Val121=)	rs1273832397
NM_003001.5(SDHC):c.367C>T (p.Pro123Ser)	rs773039986
NM_003001.5(SDHC):c.406-7T>A	rs1672546572

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