List of variants in gene SDHC reported as uncertain significance by GeneDx

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: 36

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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.450G>A (p.Gln150=)	rs749159544	0.00005
NM_003001.5(SDHC):c.118C>T (p.Arg40Trp)	rs978019587	0.00004
NM_003001.5(SDHC):c.292T>G (p.Ser98Ala)	rs371462564	0.00002
NM_003001.5(SDHC):c.14T>C (p.Leu5Ser)	rs1277411736	0.00001
NM_003001.5(SDHC):c.15G>T (p.Leu5Phe)	rs771746264	0.00001
NM_003001.5(SDHC):c.221C>T (p.Thr74Ile)	rs1332910409	0.00001
NM_003001.5(SDHC):c.25G>A (p.Val9Ile)	rs774768866	0.00001
NM_003001.5(SDHC):c.263C>T (p.Ser88Leu)	rs778212096	0.00001
NM_003001.5(SDHC):c.295T>C (p.Tyr99His)	rs760678574	0.00001
NM_003001.5(SDHC):c.42C>T (p.Leu14=)	rs1331533952	0.00001
NM_003001.5(SDHC):c.64C>T (p.Leu22Phe)	rs1473438869	0.00001
NM_003001.5(SDHC):c.7G>A (p.Ala3Thr)	rs748243732	0.00001
NM_003001.5(SDHC):c.85C>G (p.Pro29Ala)	rs878854588	0.00001
NM_003001.5(SDHC):c.8C>T (p.Ala3Val)	rs142139022	0.00001
NM_003001.5(SDHC):c.13T>A (p.Leu5Met)	rs894925936
NM_003001.5(SDHC):c.160C>A (p.Pro54Thr)	rs1553262444
NM_003001.5(SDHC):c.164A>G (p.His55Arg)	rs878854585
NM_003001.5(SDHC):c.180-3C>T	rs1328389180
NM_003001.5(SDHC):c.29G>C (p.Gly10Ala)	rs1670923061
NM_003001.5(SDHC):c.329C>T (p.Pro110Leu)	rs776485432
NM_003001.5(SDHC):c.32G>A (p.Arg11His)	rs767802663
NM_003001.5(SDHC):c.32G>T (p.Arg11Leu)	rs767802663
NM_003001.5(SDHC):c.350A>G (p.Lys117Arg)	rs1571890337
NM_003001.5(SDHC):c.367C>T (p.Pro123Ser)	rs773039986
NM_003001.5(SDHC):c.372C>A (p.Leu124=)	rs766007157
NM_003001.5(SDHC):c.379C>A (p.His127Asn)	rs1485675090
NM_003001.5(SDHC):c.387G>C (p.Trp129Cys)	rs981049067
NM_003001.5(SDHC):c.422A>G (p.Lys141Arg)	rs1558185879
NM_003001.5(SDHC):c.43C>G (p.Arg15Gly)	rs201286421
NM_003001.5(SDHC):c.457G>A (p.Val153Met)
NM_003001.5(SDHC):c.56G>T (p.Ser19Ile)
NM_003001.5(SDHC):c.59C>G (p.Pro20Arg)	rs2102295625
NM_003001.5(SDHC):c.7G>T (p.Ala3Ser)	rs748243732
NM_003001.5(SDHC):c.82G>C (p.Val28Leu)	rs754818119

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