List of variants reported as pathogenic for adrenal gland cancer by Fulgent Genetics, Fulgent Genetics

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_004168.4(SDHA):c.91C>T (p.Arg31Ter)	rs142441643	0.00025
NM_004168.4(SDHA):c.1534C>T (p.Arg512Ter)	rs748089700	0.00005
NM_004168.4(SDHA):c.223C>T (p.Arg75Ter)	rs781764920	0.00003
NM_000546.6(TP53):c.743G>A (p.Arg248Gln)	rs11540652	0.00002
NM_000546.6(TP53):c.1010G>A (p.Arg337His)	rs121912664	0.00001
NM_000546.6(TP53):c.473G>A (p.Arg158His)	rs587782144	0.00001
NM_000546.6(TP53):c.524G>A (p.Arg175His)	rs28934578	0.00001
NM_000546.6(TP53):c.659A>G (p.Tyr220Cys)	rs121912666	0.00001
NM_000546.6(TP53):c.733G>A (p.Gly245Ser)	rs28934575	0.00001
NM_003000.3(SDHB):c.137G>A (p.Arg46Gln)	rs772551056	0.00001
NM_003000.3(SDHB):c.268C>T (p.Arg90Ter)	rs74315366	0.00001
NM_003000.3(SDHB):c.380T>G (p.Ile127Ser)	rs786201095	0.00001
NM_003000.3(SDHB):c.423+1G>A	rs398122805	0.00001
NM_003000.3(SDHB):c.689G>A (p.Arg230His)	rs587782604	0.00001
NM_000546.6(TP53):c.1024C>T (p.Arg342Ter)	rs730882029
NM_000546.6(TP53):c.389T>C (p.Leu130Pro)	rs1131691013
NM_000546.6(TP53):c.559+1G>A	rs1131691042
NM_000546.6(TP53):c.817C>G (p.Arg273Gly)	rs121913343
NM_000546.6(TP53):c.818G>A (p.Arg273His)	rs28934576
NM_000546.6(TP53):c.818G>T (p.Arg273Leu)	rs28934576
NM_000546.6(TP53):c.845G>C (p.Arg282Pro)	rs730882008
NM_000546.6(TP53):c.96+1G>T	rs1131691003
NM_003000.3(SDHB):c.166_170del (p.Pro56fs)	rs786202100
NM_003000.3(SDHB):c.541-2A>G	rs786201161
NM_003000.3(SDHB):c.574T>C (p.Cys192Arg)	rs786202732
NM_003000.3(SDHB):c.640C>T (p.Gln214Ter)	rs876658461

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