List of variants in gene SDHB reported as uncertain significance for not provided

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: 75

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.8C>G (p.Ala3Gly)	rs11203289	0.01309
NM_003000.3(SDHB):c.487T>C (p.Ser163Pro)	rs33927012	0.00921
NM_003000.3(SDHB):c.21C>T (p.Leu7=)	rs147815442	0.00054
NM_003000.3(SDHB):c.403G>A (p.Val135Met)	rs201585157	0.00012
NM_003000.3(SDHB):c.455C>T (p.Ser152Phe)	rs200414835	0.00012
NM_003000.3(SDHB):c.440A>G (p.Tyr147Cys)	rs774568101	0.00010
NM_003000.3(SDHB):c.178A>G (p.Thr60Ala)	rs34599281	0.00007
NM_003000.3(SDHB):c.112C>T (p.Arg38Cys)	rs202119350	0.00006
NM_003000.3(SDHB):c.317A>G (p.Asn106Ser)	rs934514080	0.00006
NM_003000.3(SDHB):c.269G>A (p.Arg90Gln)	rs570278423	0.00004
NM_003000.3(SDHB):c.307A>G (p.Met103Val)	rs140178341	0.00004
NM_003000.3(SDHB):c.530G>A (p.Arg177His)	rs150437793	0.00004
NM_003000.3(SDHB):c.709C>T (p.Pro237Ser)	rs186768244	0.00004
NM_003000.3(SDHB):c.-5C>T	rs200890535	0.00003
NM_003000.3(SDHB):c.-6G>A	rs2295056	0.00003
NM_003000.3(SDHB):c.136C>T (p.Arg46Ter)	rs74315370	0.00003
NM_003000.3(SDHB):c.200+4A>C	rs774908929	0.00003
NM_003000.3(SDHB):c.304G>A (p.Ala102Thr)	rs777578399	0.00003
NM_003000.3(SDHB):c.344G>A (p.Arg115Gln)	rs200973284	0.00003
NM_003000.3(SDHB):c.544G>A (p.Gly182Arg)	rs201928318	0.00003
NM_003000.3(SDHB):c.650G>A (p.Arg217His)	rs747518441	0.00003
NM_003000.3(SDHB):c.130A>G (p.Ile44Val)	rs200418115	0.00002
NM_003000.3(SDHB):c.529C>T (p.Arg177Cys)	rs149091125	0.00002
NM_003000.3(SDHB):c.736A>G (p.Ile246Val)	rs146800605	0.00002
NM_003000.3(SDHB):c.739A>G (p.Met247Val)	rs200896502	0.00002
NM_003000.3(SDHB):c.820A>G (p.Lys274Glu)	rs1273897502	0.00002
NM_003000.3(SDHB):c.14T>G (p.Val5Gly)	rs760565241	0.00001
NM_003000.3(SDHB):c.172A>G (p.Met58Val)	rs1201188410	0.00001
NM_003000.3(SDHB):c.214G>A (p.Val72Ile)	rs1060503766	0.00001
NM_003000.3(SDHB):c.299C>G (p.Ser100Cys)	rs121917755	0.00001
NM_003000.3(SDHB):c.31C>T (p.Arg11Cys)	rs200868378	0.00001
NM_003000.3(SDHB):c.323G>A (p.Gly108Asp)	rs767062764	0.00001
NM_003000.3(SDHB):c.362T>C (p.Leu121Pro)	rs775925040	0.00001
NM_003000.3(SDHB):c.458T>C (p.Ile153Thr)	rs1396860069	0.00001
NM_003000.3(SDHB):c.47C>G (p.Thr16Arg)	rs775350144	0.00001
NM_003000.3(SDHB):c.523G>C (p.Glu175Gln)	rs202203339	0.00001
NM_003000.3(SDHB):c.527A>G (p.Glu176Gly)	rs201082445	0.00001
NM_003000.3(SDHB):c.541G>A (p.Asp181Asn)	rs201385062	0.00001
NM_003000.3(SDHB):c.553G>A (p.Glu185Lys)	rs1045881797	0.00001
NM_003000.3(SDHB):c.581C>G (p.Thr194Ser)	rs200535030	0.00001
NM_003000.3(SDHB):c.607G>A (p.Gly203Arg)	rs201517260	0.00001
NM_003000.3(SDHB):c.629C>T (p.Ala210Val)	rs1252727177	0.00001
NM_003000.3(SDHB):c.635T>A (p.Leu212His)	rs1307247907	0.00001
NM_003000.3(SDHB):c.638T>C (p.Met213Thr)	rs202014362	0.00001
NM_003000.3(SDHB):c.700C>T (p.Leu234=)	rs201728852	0.00001
NM_003000.3(SDHB):c.-5C>G
NM_003000.3(SDHB):c.135_136insACAAGTTGAAACT (p.Arg46delinsThrSerTer)	rs1557746639
NM_003000.3(SDHB):c.177G>C (p.Gln59His)	rs1277374324
NM_003000.3(SDHB):c.188T>C (p.Val63Ala)	rs1230335211
NM_003000.3(SDHB):c.193C>G (p.Leu65Val)	rs786202185
NM_003000.3(SDHB):c.200+5G>C	rs1553178726
NM_003000.3(SDHB):c.20T>C (p.Leu7Pro)
NM_003000.3(SDHB):c.21C>G (p.Leu7=)	rs147815442
NM_003000.3(SDHB):c.23C>T (p.Ser8Phe)	rs199848267
NM_003000.3(SDHB):c.251A>C (p.Asp84Ala)	rs864321637
NM_003000.3(SDHB):c.254C>G (p.Ser85Cys)
NM_003000.3(SDHB):c.35G>T (p.Arg12Leu)	rs1293365726
NM_003000.3(SDHB):c.379A>C (p.Ile127Leu)	rs201372280
NM_003000.3(SDHB):c.395A>G (p.His132Arg)	rs74315372
NM_003000.3(SDHB):c.397A>G (p.Met133Val)	rs1392546433
NM_003000.3(SDHB):c.446A>G (p.Gln149Arg)	rs1570947984
NM_003000.3(SDHB):c.464C>G (p.Pro155Arg)
NM_003000.3(SDHB):c.493G>A (p.Glu165Lys)	rs2101521665
NM_003000.3(SDHB):c.506A>G (p.Gln169Arg)
NM_003000.3(SDHB):c.520A>G (p.Ile174Val)	rs969943651
NM_003000.3(SDHB):c.577A>G (p.Ser193Gly)
NM_003000.3(SDHB):c.582C>T (p.Thr194=)	rs775450654
NM_003000.3(SDHB):c.642+4A>G	rs1225871505
NM_003000.3(SDHB):c.643-10G>A	rs1553177293
NM_003000.3(SDHB):c.659T>C (p.Ile220Thr)	rs878854578
NM_003000.3(SDHB):c.701T>A (p.Leu234Gln)	rs786202913
NM_003000.3(SDHB):c.705G>C (p.Gln235His)	rs1570944851
NM_003000.3(SDHB):c.716C>G (p.Ser239Cys)	rs201098090
NM_003000.3(SDHB):c.79C>G (p.Arg27Gly)	rs74315369
NM_003000.3(SDHB):c.812C>T (p.Ala271Val)	rs2077945936

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