ClinVar Miner

List of variants reported as likely pathogenic for Lung adenocarcinoma

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Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_005228.5(EGFR):c.2369C>T (p.Thr790Met) rs121434569 0.00005
NM_005228.5(EGFR):c.2326C>T (p.Arg776Cys) rs1275022697 0.00001
NM_000546.6(TP53):c.314G>T (p.Gly105Val) rs587781504
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.1781A>G (p.Asp594Gly) rs121913338
NM_004333.6(BRAF):c.1801A>G (p.Lys601Glu) rs121913364
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.2314_2325dup (p.Tyr772_Ala775dup) rs397516977
NM_004448.4(ERBB2):c.2331_2339dup (p.Gly778_Pro780dup) rs397516981
NM_004562.3(PRKN):c.601_602insA (p.Cys201Ter) rs1231455463
NM_005228.5(EGFR):c.2126A>C (p.Glu709Ala) rs397517085
NM_005228.5(EGFR):c.2155G>A (p.Gly719Ser) rs28929495
NM_005228.5(EGFR):c.2235_2249del (p.Glu746_Ala750del) rs121913421
NM_005228.5(EGFR):c.2236_2250del (p.Glu746_Ala750del) rs727504233
NM_005228.5(EGFR):c.2237_2255delinsT (p.Glu746_Ser752delinsVal) rs727504258
NM_005228.5(EGFR):c.2239_2248delinsC (p.Leu747_Ala750delinsPro) rs727504278
NM_005228.5(EGFR):c.2239_2256del (p.Leu747_Ser752del) rs121913440
NM_005228.5(EGFR):c.2239_2256delinsCAA (p.Leu747_Ser752delinsGln) rs2128954790
NM_005228.5(EGFR):c.2240_2254del (p.Leu747_Thr751del) rs121913442
NM_005228.5(EGFR):c.2240_2257del (p.Leu747_Pro753delinsSer) rs121913438
NM_005228.5(EGFR):c.2252_2277delinsAT (p.Thr751_Ile759delinsAsn) rs397517100
NM_005228.5(EGFR):c.2303_2311dup (p.Ser768_Asp770dup) rs397517109
NM_005228.5(EGFR):c.2309_2310insGTC (p.Asp770delinsGluSer) rs1554350382
NM_005228.5(EGFR):c.2318_2320delinsTCA (p.His773_Val774delinsLeuMet) rs2534769494
NM_005228.5(EGFR):c.2497T>G (p.Leu833Val) rs397517126
NM_005228.5(EGFR):c.2499G>T (p.Leu833Phe) rs2128964427
NM_005228.5(EGFR):c.2500G>T (p.Val834Leu) rs397517127
NM_005228.5(EGFR):c.2504A>T (p.His835Leu) rs397517128
NM_005228.5(EGFR):c.2555A>C (p.Lys852Thr) rs1292517709
NM_005228.5(EGFR):c.2573T>G (p.Leu858Arg) rs121434568
NM_005228.5(EGFR):c.2582T>A (p.Leu861Gln) rs121913444
NM_005228.5(EGFR):c.709_710delinsTT (p.Ala237Phe) rs2535499036
NM_016507.4(CDK12):c.2636G>T (p.Gly879Val) rs1131692238
t(8;10)(q12.1;q23.31)

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