ClinVar Miner

List of variants in gene combination HRAS, LRRC56 studied for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 70
Download table as spreadsheet
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.450+171C>T rs376091236 0.00025
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.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.520C>T (p.Pro174Ser) rs397517144 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.505C>T (p.Arg169Trp) rs151229168 0.00003
NM_005343.4(HRAS):c.54G>A (p.Ala18=) rs148380285 0.00003
NM_005343.4(HRAS):c.57G>C (p.Leu19=) rs761648389 0.00003
NM_005343.4(HRAS):c.*1C>T rs730880327 0.00002
NM_005343.4(HRAS):c.358C>T (p.Leu120=) rs397517139 0.00002
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.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.112-13T>A rs766582484 0.00001
NM_005343.4(HRAS):c.11A>G (p.Tyr4Cys) rs764622691 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.304C>T (p.Arg102Trp) rs1057517913 0.00001
NM_005343.4(HRAS):c.31G>A (p.Ala11Thr) rs727504496 0.00001
NM_005343.4(HRAS):c.378A>G (p.Glu126=) rs397517140 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.468C>T (p.Phe156=) rs770648642 0.00001
NM_005343.4(HRAS):c.482G>A (p.Arg161His) rs748729430 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
NC_000011.9:g.(?_532631)_(534375_?)dup
NM_005343.4(HRAS):c.*5+14C>A rs587780953
NM_005343.4(HRAS):c.-2C>A rs757657838
NM_005343.4(HRAS):c.-5G>A rs879083675
NM_005343.4(HRAS):c.-95CGGCCC[1] rs112488103
NM_005343.4(HRAS):c.112-4G>A rs1589792986
NM_005343.4(HRAS):c.162C>T (p.Asp54=) rs1057520410
NM_005343.4(HRAS):c.165_166insTCCGGAAGCAGGTGGTCATTGATGGGGAGACGTGCCTGTTGGACATC (p.Leu56fs) rs1851284408
NM_005343.4(HRAS):c.192C>T (p.Tyr64=) rs2133990881
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.291-17C>G rs753558541
NM_005343.4(HRAS):c.291-6T>G rs766909143
NM_005343.4(HRAS):c.291-9A>G rs1564789180
NM_005343.4(HRAS):c.36C>A (p.Gly12=) rs727504424
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_005343.4(HRAS):c.473C>T (p.Thr158Met) rs587778400
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.451-12_451del rs2133985401
NM_176795.5(HRAS):c.500C>T (p.Pro167Leu) rs730880457

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.