ClinVar Miner

List of variants reported as likely pathogenic for Vascular Tumors Including Pyogenic Granuloma

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Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_004985.5(KRAS):c.35G>A (p.Gly12Asp) rs121913529 0.00001
NM_002524.5(NRAS):c.181C>A (p.Gln61Lys) rs121913254
NM_005343.4(HRAS):c.145G>A (p.Glu49Lys) rs1277340795
NM_005343.4(HRAS):c.182A>G (p.Gln61Arg) rs121913233
NM_005343.4(HRAS):c.37G>A (p.Gly13Ser) rs104894228

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