ClinVar Miner

List of variants in gene SDHD reported as uncertain significance for Hereditary Paraganglioma-Pheochromocytoma Syndromes

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Total variants: 22
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HGVS dbSNP
NM_003002.4(SDHD):c.*111A>G
NM_003002.4(SDHD):c.*302A>G rs201163059
NM_003002.4(SDHD):c.*587A>G rs886047701
NM_003002.4(SDHD):c.*648A>G rs201560447
NM_003002.4(SDHD):c.*663A>G rs200264243
NM_003002.4(SDHD):c.*669T>C
NM_003002.4(SDHD):c.*71C>A rs886047700
NM_003002.4(SDHD):c.*738T>A rs886047702
NM_003002.4(SDHD):c.*762A>G
NM_003002.4(SDHD):c.*815T>C rs886047703
NM_003002.4(SDHD):c.*93A>G
NM_003002.4(SDHD):c.136G>A (p.Val46Met) rs886047699
NM_003002.4(SDHD):c.148C>G (p.His50Asp) rs779249550
NM_003002.4(SDHD):c.174C>T (p.Gly58=)
NM_003002.4(SDHD):c.228C>T (p.Leu76=) rs148634289
NM_003002.4(SDHD):c.239T>G (p.Leu80Arg) rs1555187010
NM_003002.4(SDHD):c.281C>G (p.Ser94Cys) rs199754684
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.445A>G (p.Ile149Val)
NM_003002.4(SDHD):c.479G>T (p.Ter160Leu) rs201372601
NM_003002.4(SDHD):c.53-6C>A

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