ClinVar Miner

List of variants reported as uncertain significance for Hereditary Paraganglioma-Pheochromocytoma Syndromes by Section on Medical Neuroendocrinolgy,National Institutes of Health

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Total variants: 8
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HGVS dbSNP
NM_003000.2(SDHB):c.445C>T (p.Gln149Ter) rs876658451
NM_003000.2(SDHB):c.642G>C (p.Gln214His) rs1278834014
NM_003001.5(SDHC):c.218G>A (p.Gly73Asp) rs1553264219
NM_003002.4(SDHD):c.148C>G (p.His50Asp) rs779249550
NM_003002.4(SDHD):c.239T>G (p.Leu80Arg) rs1555187010
NM_003002.4(SDHD):c.328_330GTT[1] (p.Val111del) rs1555187580
NM_003002.4(SDHD):c.443G>T (p.Gly148Val) rs1555187633
NM_003002.4(SDHD):c.479G>T (p.Ter160Leu) rs201372601

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