ClinVar Miner

List of variants in gene ACADSB reported by Breakthrough Genomics, Breakthrough Genomics

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Gene type:
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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_001609.4(ACADSB):c.*3819A>G rs3980942 0.98475
NM_001609.4(ACADSB):c.1129-90A>G rs2421166 0.98353
NM_001609.4(ACADSB):c.*3234C>G rs3763738 0.98286
NM_001609.4(ACADSB):c.*1868C>G rs10902868 0.88496
NM_001609.4(ACADSB):c.*262C>T rs12248515 0.43651
NM_001609.4(ACADSB):c.*4467A>T rs6838 0.36669
NM_001609.4(ACADSB):c.38G>A (p.Arg13Lys) rs12263012 0.30009
NM_001609.4(ACADSB):c.*545G>A rs1140593 0.23068
NM_001609.4(ACADSB):c.639C>T (p.His213=) rs1140591 0.22865
NM_001609.4(ACADSB):c.*2331C>G rs7079265 0.20119
NM_001609.4(ACADSB):c.*2175A>C rs7909871 0.20108
NM_001609.4(ACADSB):c.*4426T>C rs7732 0.19948
NM_001609.4(ACADSB):c.*2490T>C rs7914164 0.19560
NM_001609.4(ACADSB):c.*1200A>T rs11248371 0.10692
NM_001609.4(ACADSB):c.*2113G>A rs7922412 0.10328
NM_001609.4(ACADSB):c.303+125A>C rs4980246 0.07944
NM_001609.4(ACADSB):c.946A>G (p.Ile316Val) rs1131430 0.06319
NM_001609.4(ACADSB):c.*2670C>T rs144203038 0.01950
NM_001609.4(ACADSB):c.168A>G (p.Thr56=) rs34221067 0.01583
NM_001609.4(ACADSB):c.*109G>A rs34955007 0.01412
NM_001609.3(ACADSB):c.-97T>C rs148327034 0.01260
NM_001609.3(ACADSB):c.-87G>T rs150850221 0.00878
NM_001609.3(ACADSB):c.-89G>T rs141443308 0.00878
NM_001609.4(ACADSB):c.*3907C>G rs185346880 0.00584
NM_001609.4(ACADSB):c.786G>A (p.Pro262=) rs76111609 0.00373
NM_001609.4(ACADSB):c.92A>G (p.His31Arg) rs57321698 0.00270
NM_001609.4(ACADSB):c.*358T>C rs184796725 0.00207
NM_001609.4(ACADSB):c.1014C>T (p.His338=) rs57339164 0.00125
NM_001609.4(ACADSB):c.*133C>G rs58589087 0.00109
NM_001609.4(ACADSB):c.1101G>A (p.Ala367=) rs145295182 0.00010
NM_001609.4(ACADSB):c.439A>T (p.Asn147Tyr) rs747291865 0.00006
NM_001609.4(ACADSB):c.95T>A (p.Val32Asp) rs751722805 0.00001
NM_001609.3(ACADSB):c.-107G>A rs190149746
NM_001609.4(ACADSB):c.1229-84C>T rs41291346

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