ClinVar Miner

List of variants in gene combination HRAS, LRRC56 reported as benign for not specified

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Gene type:
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Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_005343.4(HRAS):c.81T>C (p.His27=) rs12628 0.34645
NM_005343.4(HRAS):c.111+15G>A rs41258054 0.04363
NM_005343.4(HRAS):c.-10C>T rs41294870 0.03593
NM_005343.4(HRAS):c.477G>A (p.Leu159=) rs140060409 0.00222
NM_005343.4(HRAS):c.357C>T (p.Asp119=) rs111352454 0.00121
NM_005343.4(HRAS):c.257A>C (p.Asn86Thr) rs138272051 0.00019
NM_005343.4(HRAS):c.330C>T (p.Pro110=) rs200747280 0.00011
NM_005343.4(HRAS):c.177C>T (p.Ala59=) rs730880456 0.00010
NM_005343.4(HRAS):c.*5+20C>T rs756277885 0.00007
NM_005343.4(HRAS):c.520C>T (p.Pro174Ser) rs397517144 0.00004
NM_005343.4(HRAS):c.54G>A (p.Ala18=) rs148380285 0.00003
NM_005343.4(HRAS):c.*1C>T rs730880327 0.00002
NM_005343.4(HRAS):c.510G>A (p.Lys170=) rs397517143 0.00001
NM_005343.4(HRAS):c.*5+14C>A rs587780953
NM_005343.4(HRAS):c.-95CGGCCC[1] rs112488103
NM_005343.4(HRAS):c.291-6T>G rs766909143

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