List of variants reported as likely pathogenic for small intestine neoplasm by Baylor Genetics

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.650G>A (p.Arg217His)	rs747518441	0.00003
NM_003001.5(SDHC):c.377A>G (p.Tyr126Cys)	rs898854295	0.00003
NM_003000.3(SDHB):c.221A>C (p.Asp74Ala)	rs876658713	0.00001
NM_003000.3(SDHB):c.286G>A (p.Gly96Ser)	rs587782243	0.00001
NM_003000.3(SDHB):c.649C>T (p.Arg217Cys)	rs200245469	0.00001
NM_003001.5(SDHC):c.148C>T (p.Arg50Cys)	rs587778661	0.00001
NM_003001.5(SDHC):c.215G>A (p.Arg72His)	rs778582853	0.00001
NM_003000.3(SDHB):c.289A>T (p.Ile97Phe)	rs1553177769
NM_003000.3(SDHB):c.292T>C (p.Cys98Arg)
NM_003000.3(SDHB):c.640C>T (p.Gln214Ter)	rs876658461
NM_003000.3(SDHB):c.689G>T (p.Arg230Leu)	rs587782604
NM_003001.5(SDHC):c.179+1G>T	rs1057517818
NM_003001.5(SDHC):c.387G>A (p.Trp129Ter)	rs981049067

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