ClinVar Miner

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

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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_005343.4(HRAS):c.451-48C>T rs45607337 0.01453
NM_005343.4(HRAS):c.451-341G>A rs45489193 0.00945
NM_005343.4(HRAS):c.*76G>C rs45565838 0.00511
NC_000011.10:g.531070G>A rs534235694 0.00340
NC_000011.10:g.530466G>C rs569269635 0.00307
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.177C>T (p.Ala59=) rs730880456 0.00010
NM_005343.4(HRAS):c.450+174G>A rs371117417 0.00008
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.222C>T (p.Thr74=) rs372223975 0.00005
NM_005343.4(HRAS):c.508A>T (p.Lys170Ter) rs372936166 0.00005
NM_005343.4(HRAS):c.534C>G (p.Gly178=) rs770431635 0.00004
NM_005343.4(HRAS):c.291-8C>T rs1057522962 0.00003
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.45C>T (p.Gly15=) rs727504614 0.00002
NM_005343.4(HRAS):c.*5+14C>G rs587780953 0.00001
NM_005343.4(HRAS):c.-19C>T rs1187467800 0.00001
NM_005343.4(HRAS):c.120C>T (p.Tyr40=) rs763920334 0.00001
NM_005343.4(HRAS):c.150G>A (p.Thr50=) rs1057520421 0.00001
NM_005343.4(HRAS):c.219C>T (p.Arg73=) rs749870259 0.00001
NM_005343.4(HRAS):c.228G>A (p.Glu76=) rs1057522598 0.00001
NM_005343.4(HRAS):c.24G>C (p.Val8=) rs1451160542 0.00001
NM_005343.4(HRAS):c.302A>G (p.Lys101Arg) rs1131691997 0.00001
NM_005343.4(HRAS):c.426C>T (p.Ile142=) rs533567288 0.00001
NM_005343.4(HRAS):c.450+18C>T rs1057522255 0.00001
NM_005343.4(HRAS):c.537C>T (p.Pro179=) rs371316832 0.00001
NM_005343.4(HRAS):c.64C>T (p.Gln22Ter) rs121917757 0.00001
NM_176795.5(HRAS):c.480C>T (p.Ser160=) rs1057522069 0.00001
NM_176795.5(HRAS):c.498C>G (p.Pro166=) rs377676071 0.00001
NM_176795.5(HRAS):c.501G>A (p.Pro167=) rs764211685 0.00001
NC_000011.10:g.528639C>T
NC_000011.10:g.528669C>T
NC_000011.10:g.529719C>G
NC_000011.10:g.530428_530455del
NC_000011.10:g.530428_530483del
NC_000011.10:g.530444G>A
NC_000011.10:g.530447A>G rs199711118
NC_000011.10:g.530475G>A rs111377659
NC_000011.10:g.530522G>C
NC_000011.10:g.530614G>C
NC_000011.10:g.530894G>C
NC_000011.10:g.531063G>C
NC_000011.10:g.531072G>A
NC_000011.10:g.531174C>G
NM_005343.4(HRAS):c.102C>G (p.Pro34=) rs149199691
NM_005343.4(HRAS):c.234C>T (p.Phe78=) rs1057522882
NM_005343.4(HRAS):c.312G>A (p.Lys104=) rs1060504682
NM_005343.4(HRAS):c.451-5C>T rs370181298
NM_005343.4(HRAS):c.483T>G (p.Arg161=)
NM_005343.4(HRAS):c.96C>T (p.Tyr32=) rs369039481

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