ClinVar Miner

List of variants studied for Glioma susceptibility 1

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Total variants: 8
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HGVS dbSNP gnomAD frequency
NM_138711.6(PPARG):c.1341C>T (p.His447=) rs3856806 0.11181
NM_000546.6(TP53):c.375G>A (p.Thr125=) rs55863639 0.00001
NM_001018113.3(FANCB):c.1327-1G>A rs1295003944 0.00001
NM_005896.4(IDH1):c.394C>T (p.Arg132Cys) rs121913499 0.00001
NM_005896.4(IDH1):c.395G>A (p.Arg132His) rs121913500 0.00001
NM_000546.6(TP53):c.454C>T (p.Pro152Ser) rs767328513
NM_000546.6(TP53):c.542G>T (p.Arg181Leu) rs397514495
NM_004448.4(ERBB2):c.2740G>A (p.Glu914Lys) rs28933368

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