ClinVar Miner

List of variants reported as likely pathogenic for Gastrointestinal stroma tumor; Paragangliomas 4; Pheochromocytoma

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Total variants: 13
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HGVS dbSNP
NM_003000.2(SDHB):c.143A>T (p.Asp48Val) rs202101384
NM_003000.2(SDHB):c.1A>T (p.Met1Leu) rs1131691049
NM_003000.2(SDHB):c.201-2A>C rs878854574
NM_003000.2(SDHB):c.201-?_765+?dup
NM_003000.2(SDHB):c.286G>A (p.Gly96Ser) rs587782243
NM_003000.2(SDHB):c.590C>G (p.Pro197Arg) rs74315367
NM_003000.2(SDHB):c.598T>C (p.Trp200Arg) rs1557739966
NM_003000.2(SDHB):c.649C>T (p.Arg217Cys) rs200245469
NM_003000.2(SDHB):c.724C>A (p.Arg242Ser) rs786203251
NM_003000.2(SDHB):c.73-1G>T
NM_003000.2(SDHB):c.780dup (p.Lys261fs) rs1557738304
NM_003000.2(SDHB):c.784_787dup (p.Ile263fs) rs1553176976
NM_003000.2(SDHB):c.785_786insG (p.Ile263fs) rs1553176979

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