List of variants in gene SDHA reported as uncertain significance by Sema4, Sema4

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.1919A>G (p.Glu640Gly)	rs372480044	0.00058
NM_004168.4(SDHA):c.704T>C (p.Ile235Thr)	rs144513891	0.00015
NM_004168.4(SDHA):c.1591G>A (p.Val531Met)	rs371056571	0.00009
NM_004168.4(SDHA):c.1532T>C (p.Leu511Pro)	rs375194444	0.00008
NM_004168.4(SDHA):c.1064+5G>A	rs200021115	0.00006
NM_004168.4(SDHA):c.1724C>T (p.Ala575Val)	rs750327309	0.00004
NM_004168.4(SDHA):c.5C>T (p.Ser2Leu)	rs780064103	0.00004
NM_004168.4(SDHA):c.1196C>A (p.Pro399Gln)	rs878854625	0.00001
NM_004168.4(SDHA):c.1352G>A (p.Arg451His)	rs370690436	0.00001
NM_004168.4(SDHA):c.422A>G (p.Tyr141Cys)	rs1377816261	0.00001
NM_004168.4(SDHA):c.568T>C (p.Cys190Arg)	rs908267345	0.00001
NM_004168.4(SDHA):c.771-17_771-11del	rs1216026111	0.00001
NM_004168.4(SDHA):c.896-11G>T	rs774043076	0.00001
NM_004168.4(SDHA):c.919A>G (p.Ile307Val)	rs200632016	0.00001
NM_004168.4(SDHA):c.92G>A (p.Arg31Gln)	rs752532780	0.00001
NM_004168.4(SDHA):c.1177G>T (p.Val393Leu)	rs372989971
NM_004168.4(SDHA):c.1337T>C (p.Val446Ala)	rs201741295
NM_004168.4(SDHA):c.1360G>A (p.Ala454Thr)	rs1057517550
NM_004168.4(SDHA):c.1375G>C (p.Asp459His)	rs1735797208
NM_004168.4(SDHA):c.1399T>A (p.Cys467Ser)	rs1315131938
NM_004168.4(SDHA):c.1547A>G (p.Gln516Arg)	rs981171929
NM_004168.4(SDHA):c.1793A>G (p.Lys598Arg)	rs1579439363
NM_004168.4(SDHA):c.319A>G (p.Ile107Val)	rs1060503720
NM_004168.4(SDHA):c.397C>G (p.Leu133Val)	rs2126547261
NM_004168.4(SDHA):c.44G>C (p.Arg15Pro)	rs1060503707
NM_004168.4(SDHA):c.510G>C (p.Gln170His)	rs1579385651
NM_004168.4(SDHA):c.683A>G (p.Asn228Ser)	rs2126558564

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