ClinVar Miner

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

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Gene type:
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Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_005343.4(HRAS):c.477G>A (p.Leu159=) rs140060409 0.00222
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.369C>T (p.Arg123=) rs200945755 0.00006
NM_005343.4(HRAS):c.42G>A (p.Val14=) rs777038147 0.00006
NM_005343.4(HRAS):c.-54+7G>A rs1183370084 0.00004
NM_005343.4(HRAS):c.249C>T (p.Ala83=) rs111372582 0.00004
NM_005343.4(HRAS):c.363T>C (p.Ala121=) rs146440188 0.00004
NM_005343.4(HRAS):c.534C>G (p.Gly178=) rs770431635 0.00004
NM_005343.4(HRAS):c.282C>T (p.His94=) rs375893752 0.00003
NM_005343.4(HRAS):c.412G>A (p.Gly138Ser) rs397517142 0.00003
NM_005343.4(HRAS):c.57G>C (p.Leu19=) rs761648389 0.00003
NM_005343.4(HRAS):c.358C>T (p.Leu120=) rs397517139 0.00002
NM_005343.4(HRAS):c.45C>T (p.Gly15=) rs727504614 0.00002
NM_005343.4(HRAS):c.84T>C (p.Phe28=) rs915086641 0.00002
NM_005343.4(HRAS):c.*6-2A>C rs730880459 0.00001
NM_005343.4(HRAS):c.111+14C>T rs372917082 0.00001
NM_005343.4(HRAS):c.112-10C>T rs727503092 0.00001
NM_005343.4(HRAS):c.141T>C (p.Asp47=) rs765092617 0.00001
NM_005343.4(HRAS):c.171T>C (p.Asp57=) rs776105083 0.00001
NM_005343.4(HRAS):c.378A>G (p.Glu126=) rs397517140 0.00001
NM_005343.4(HRAS):c.468C>T (p.Phe156=) rs770648642 0.00001
NM_005343.4(HRAS):c.510G>A (p.Lys170=) rs397517143 0.00001
NM_005343.4(HRAS):c.516C>T (p.Asn172=) rs765180494 0.00001
NM_005343.4(HRAS):c.162C>T (p.Asp54=) rs1057520410
NM_005343.4(HRAS):c.192C>T (p.Tyr64=) rs2133990881
NM_005343.4(HRAS):c.291-17C>G rs753558541
NM_005343.4(HRAS):c.69G>A (p.Leu23=) rs1589793671
NM_005343.4(HRAS):c.96C>T (p.Tyr32=) rs369039481
NM_176795.5(HRAS):c.500C>T (p.Pro167Leu) rs730880457

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