ClinVar Miner

List of variants reported as likely pathogenic for Non-small cell lung cancer

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Total variants: 56
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HGVS dbSNP
NM_000455.4(STK11):c.587G>T (p.Gly196Val) rs1057519858
NM_001626.6(AKT2):c.1112G>A (p.Arg371His) rs778561687
NM_002524.5(NRAS):c.182A>C (p.Gln61Pro) rs11554290
NM_004333.6(BRAF):c.1396G>A (p.Gly466Arg) rs121913353
NM_004333.6(BRAF):c.1397G>T (p.Gly466Val) rs121913351
NM_004333.6(BRAF):c.1405G>A (p.Gly469Arg) rs121913357
NM_004333.6(BRAF):c.1742A>G (p.Asn581Ser) rs121913370
NM_004333.6(BRAF):c.1780G>A (p.Asp594Asn) rs397516896
NM_004333.6(BRAF):c.1798G>A (p.Val600Met) rs121913378
NM_004333.6(BRAF):c.1798G>T (p.Val600Leu) rs121913378
NM_004333.6(BRAF):c.1799_1801del (p.Val600_Lys601delinsGlu) rs397516897
NM_004448.3(ERBB2):c.2313_2324dup (p.Tyr772_Ala775dup) rs397516975
NM_004448.3(ERBB2):c.2314_2325dup (p.Tyr772_Ala775dup) rs397516977
NM_004448.3(ERBB2):c.2320del (p.Met774fs) rs397516978
NM_004448.3(ERBB2):c.2324_2325insCTCCGTGATGGC (p.Gly776_Val777insSerValMetAla) rs397516976
NM_004448.3(ERBB2):c.2325_2326insTCCGTGATGGCT (p.Gly776_Val777insSerValMetAla) rs1555618025
NM_004448.3(ERBB2):c.2326_2327insTGT (p.Gly776delinsValCys) rs397516979
NM_004448.3(ERBB2):c.2326_2327insTTT (p.Gly776delinsValCys) rs397516979
NM_004448.3(ERBB2):c.2326delinsTTAT (p.Gly776delinsLeuCys) rs397516980
NM_004448.3(ERBB2):c.2332_2340dup (p.Gly778_Pro780dup) rs397516982
NM_004985.5(KRAS):c.179G>T (p.Gly60Val) rs727503108
NM_004985.5(KRAS):c.290G>A (p.Arg97Lys) rs727503106
NM_004985.5(KRAS):c.35G>T (p.Gly12Val) rs121913529
NM_004985.5(KRAS):c.39C>A (p.Gly13=) rs397517040
NM_004985.5(KRAS):c.39C>T (p.Gly13=) rs397517040
NM_005228.5(EGFR):c.2155G>C (p.Gly719Arg) rs28929495
NM_005228.5(EGFR):c.2156G>A (p.Gly719Asp) rs121913428
NM_005228.5(EGFR):c.2193G>A (p.Trp731Ter) rs121913467
NM_005228.5(EGFR):c.2198C>T (p.Pro733Leu) rs121913446
NM_005228.5(EGFR):c.2200G>A (p.Glu734Lys) rs121913420
NM_005228.5(EGFR):c.2203G>A (p.Gly735Ser) rs121913430
NM_005228.5(EGFR):c.2225T>C (p.Val742Ala) rs121913466
NM_005228.5(EGFR):c.2232_2249delinsAAA (p.Glu746_Ala750del) rs397517094
NM_005228.5(EGFR):c.2236G>A (p.Glu746Lys) rs121913427
NM_005228.5(EGFR):c.2240_2248del (p.Leu747_Ala750delinsSer) rs397517098
NM_005228.5(EGFR):c.2248G>C (p.Ala750Pro) rs121913229
NM_005228.5(EGFR):c.2255C>A (p.Ser752Tyr) rs121913464
NM_005228.5(EGFR):c.2257C>T (p.Pro753Ser) rs121913231
NM_005228.5(EGFR):c.2281G>A (p.Asp761Asn) rs121913418
NM_005228.5(EGFR):c.2281G>T (p.Asp761Tyr) rs121913418
NM_005228.5(EGFR):c.2284-5_2290dup rs397517106
NM_005228.5(EGFR):c.2303G>T (p.Ser768Ile) rs121913465
NM_005228.5(EGFR):c.2303_2311dup (p.Ser768_Asp770dup) rs397517109
NM_005228.5(EGFR):c.2315_2320dup (p.Val774_Cys775insAlaHis) rs397517114
NM_005228.5(EGFR):c.2317_2322dup (p.His773_Val774dup) rs397517116
NM_005228.5(EGFR):c.2318A>G (p.His773Arg) rs121913432
NM_005228.5(EGFR):c.2320_2321insGCCACG (p.Val774_Cys775insGlyHis) rs1554350366
NM_005228.5(EGFR):c.2369C>T (p.Thr790Met) rs121434569
NM_005228.5(EGFR):c.2572C>A (p.Leu858Met) rs121913443
NM_005228.5(EGFR):c.2572_2573inv (p.Leu858Arg) rs1057519847
NM_005228.5(EGFR):c.2573T>A (p.Leu858Gln) rs121434568
NM_005228.5(EGFR):c.2573_2574delinsGT (p.Leu858Arg) rs1057519848
NM_005343.4(HRAS):c.175G>A (p.Ala59Thr) rs727503093
NM_006218.4(PIK3CA):c.1359_1373del (p.Glu453_Pro458delinsAsp) rs397517200
NM_006218.4(PIK3CA):c.1624G>C (p.Glu542Gln) rs121913273
NM_006218.4(PIK3CA):c.3129G>A (p.Met1043Ile) rs121913283

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