ClinVar Miner

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

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_005343.4(HRAS):c.257A>C (p.Asn86Thr) rs138272051 0.00019
NM_005343.4(HRAS):c.520C>T (p.Pro174Ser) rs397517144 0.00004
NM_005343.4(HRAS):c.505C>T (p.Arg169Trp) rs151229168 0.00003
NM_005343.4(HRAS):c.367C>T (p.Arg123Cys) rs369106578 0.00002
NM_005343.4(HRAS):c.450+17C>T rs367869009 0.00002
NM_005343.4(HRAS):c.112-13T>A rs766582484 0.00001
NM_005343.4(HRAS):c.11A>G (p.Tyr4Cys) rs764622691 0.00001
NM_005343.4(HRAS):c.304C>T (p.Arg102Trp) rs1057517913 0.00001
NM_005343.4(HRAS):c.31G>A (p.Ala11Thr) rs727504496 0.00001
NM_005343.4(HRAS):c.398T>A (p.Leu133His) rs766801436 0.00001
NM_005343.4(HRAS):c.450+84C>A rs727504926 0.00001
NM_005343.4(HRAS):c.482G>A (p.Arg161His) rs748729430 0.00001
NC_000011.9:g.(?_532631)_(534375_?)dup
NM_005343.4(HRAS):c.-2C>A rs757657838
NM_005343.4(HRAS):c.-5G>A rs879083675
NM_005343.4(HRAS):c.112-4G>A rs1589792986
NM_005343.4(HRAS):c.165_166insTCCGGAAGCAGGTGGTCATTGATGGGGAGACGTGCCTGTTGGACATC (p.Leu56fs) rs1851284408
NM_005343.4(HRAS):c.203G>A (p.Arg68Gln) rs730880461
NM_005343.4(HRAS):c.290+10G>A rs769212136
NM_005343.4(HRAS):c.290+1G>C rs1851270546
NM_005343.4(HRAS):c.291-9A>G rs1564789180
NM_005343.4(HRAS):c.37_38inv (p.Gly13Pro)
NM_005343.4(HRAS):c.401C>T (p.Ala134Val) rs397517141
NM_005343.4(HRAS):c.418C>T (p.Pro140Ser) rs144001095
NM_005343.4(HRAS):c.445C>T (p.Arg149Trp) rs1554884750
NM_005343.4(HRAS):c.450+20C>A rs201524241
NM_176795.5(HRAS):c.451-12_451del rs2133985401

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