ClinVar Miner

List of variants reported as pathogenic for Lung adenocarcinoma

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Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_005228.5(EGFR):c.2492G>A (p.Arg831His) rs150036236 0.00003
NM_005228.5(EGFR):c.988G>A (p.Glu330Lys) rs139429793 0.00001
NM_000321.3(RB1):c.380+2T>C
NM_000546.6(TP53):c.1051A>T (p.Lys351Ter)
NM_000546.6(TP53):c.622G>T (p.Asp208Tyr) rs1597368376
NM_000546.6(TP53):c.796G>T (p.Gly266Ter) rs1057519990
NM_000546.6(TP53):c.818G>A (p.Arg273His) rs28934576
NM_000546.6(TP53):c.916C>T (p.Arg306Ter) rs121913344
NM_001378902.1(ROS1):c.3388G>A (p.Gly1130Arg)
NM_001378902.1(ROS1):c.6076G>A (p.Gly2026Arg) rs1057519788
NM_004333.6(BRAF):c.1397G>T (p.Gly466Val) rs121913351
NM_004333.6(BRAF):c.1790T>G (p.Leu597Arg) rs121913366
NM_004448.4(ERBB2):c.2263_2264delinsCC (p.Leu755Pro) rs121913469
NM_004448.4(ERBB2):c.2313_2324dup (p.Tyr772_Ala775dup) rs397516975
NM_004448.4(ERBB2):c.2328_2336dup (p.Val777_Ser779dup) rs587776805
NM_004448.4(ERBB2):c.2606T>G (p.Leu869Arg) rs1131692237
NM_004465.2(FGF10):c.*1093A>G
NM_004985.5(KRAS):c.34G>T (p.Gly12Cys) rs121913530
NM_005228.5(EGFR):c.2235_2249del (p.Glu746_Ala750del) rs121913421
NM_005228.5(EGFR):c.2573T>G (p.Leu858Arg) rs121434568
NM_013988.2(PARK2):c.(8_8)_(171_171)+180544del

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