ClinVar Miner

List of variants in gene combination HRAS, LRRC56 reported as uncertain significance by GeneDx

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Gene type:
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Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_005343.4(HRAS):c.506G>A (p.Arg169Gln) rs142218590 0.00007
NM_005343.4(HRAS):c.460G>A (p.Asp154Asn) rs745497215 0.00004
NM_005343.4(HRAS):c.412G>A (p.Gly138Ser) rs397517142 0.00003
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.112-13T>A rs766582484 0.00001
NM_005343.4(HRAS):c.277A>G (p.Ile93Val) rs587782949 0.00001
NM_005343.4(HRAS):c.304C>T (p.Arg102Trp) rs1057517913 0.00001
NM_005343.4(HRAS):c.391C>T (p.Gln131Ter) rs376688893 0.00001
NM_005343.4(HRAS):c.398T>A (p.Leu133His) rs766801436 0.00001
NM_005343.4(HRAS):c.454G>A (p.Val152Met) rs1851183840 0.00001
NM_005343.4(HRAS):c.491G>A (p.Arg164Gln) rs753977266 0.00001
NM_005343.4(HRAS):c.536C>T (p.Pro179Leu) rs760429548 0.00001
NM_005343.4(HRAS):c.538G>A (p.Gly180Ser) rs772602067 0.00001
NM_005343.4(HRAS):c.-53-5G>A
NM_005343.4(HRAS):c.102C>G (p.Pro34=) rs149199691
NM_005343.4(HRAS):c.136A>G (p.Ile46Val) rs2133991578
NM_005343.4(HRAS):c.21G>C (p.Val7=)
NM_005343.4(HRAS):c.262A>T (p.Lys88Ter)
NM_005343.4(HRAS):c.317C>G (p.Ser106Trp) rs730880462
NM_005343.4(HRAS):c.362C>T (p.Ala121Val) rs376667492
NM_005343.4(HRAS):c.445C>T (p.Arg149Trp) rs1554884750
NM_005343.4(HRAS):c.448C>T (p.Gln150Ter) rs1064796999
NM_005343.4(HRAS):c.451-5C>G rs370181298
NM_005343.4(HRAS):c.481C>T (p.Arg161Cys) rs758956556
NM_005343.4(HRAS):c.484G>A (p.Glu162Lys) rs1564787942
NM_005343.4(HRAS):c.517C>T (p.Pro173Ser) rs1851178613
NM_005343.4(HRAS):c.535C>T (p.Pro179Ser) rs1201430199
NM_005343.4(HRAS):c.544A>G (p.Met182Val) rs730880465

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