ClinVar Miner

List of variants in gene combination HRAS, LRRC56 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
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.257A>C (p.Asn86Thr) rs138272051 0.00019
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.534C>G (p.Gly178=) rs770431635 0.00004
NM_005343.4(HRAS):c.54G>A (p.Ala18=) rs148380285 0.00003
NM_005343.4(HRAS):c.120C>T (p.Tyr40=) rs763920334 0.00001
NM_005343.4(HRAS):c.219C>T (p.Arg73=) rs749870259 0.00001
NM_176795.5(HRAS):c.498C>G (p.Pro166=) rs377676071 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.530447_530474del
NC_000011.10:g.530475G>A rs111377659
NC_000011.10:g.530522G>C
NC_000011.10:g.530587G>C
NC_000011.10:g.530614G>C
NC_000011.10:g.530894G>C
NC_000011.10:g.530895G>C
NC_000011.10:g.531047C>T
NC_000011.10:g.531063G>C
NC_000011.10:g.531065G>A
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.173C>T (p.Thr58Ile) rs121917758
NM_005343.4(HRAS):c.34G>T (p.Gly12Cys) rs104894229
NM_005343.4(HRAS):c.35G>A (p.Gly12Asp) rs104894230
NM_005343.4(HRAS):c.38G>A (p.Gly13Asp) rs104894226
NM_005343.4(HRAS):c.483T>G (p.Arg161=)

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