ClinVar Miner

List of variants reported as uncertain significance for Lung adenocarcinoma

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Total variants: 84
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HGVS dbSNP gnomAD frequency
NM_000264.5(PTCH1):c.68C>T (p.Ala23Val) rs761204245 0.00002
NM_005228.5(EGFR):c.2270A>G (p.Lys757Arg) rs397517102 0.00002
NM_000038.6(APC):c.1015A>T (p.Ser339Cys)
NM_000249.4(MLH1):c.1896+179G>C
NM_000249.4(MLH1):c.207+346G>C
NM_000249.4(MLH1):c.678-234_678-233insAGTG
NM_000264.5(PTCH1):c.3168+139G>C
NM_000264.5(PTCH1):c.3449+255G>T
NM_000314.8(PTEN):c.*667A>T rs886047409
NM_000321.3(RB1):c.1696-7964C>T
NM_000325.6(PITX2):c.412-283C>A
NM_000455.5(STK11):c.464+322C>T
NM_000546.6(TP53):c.1101-313G>A
NM_000546.6(TP53):c.584T>C (p.Ile195Thr) rs760043106
NM_000546.6(TP53):c.7G>C (p.Glu3Gln) rs2073524362
NM_000743.5(CHRNA3):c.378-230_378-229inv
NM_000745.4(CHRNA5):c.*552T>C
NM_000745.4(CHRNA5):c.304-96C>A
NM_000750.5(CHRNB4):c.*319_*320delinsAT
NM_000870.7(HTR4):c.1076+211C>A
NM_001005738.2(FPR2):c.-15+1402C>T
NM_001012426.2(FOXP4):c.-16-161C>A
NM_001012426.2(FOXP4):c.-17+129G>C
NM_001012426.2(FOXP4):c.-17+229T>C
NM_001012426.2(FOXP4):c.511-141G>T
NM_001012426.2(FOXP4):c.511-214T>C
NM_001243133.2(NLRP3):c.-121T>C
NM_001243133.2(NLRP3):c.-146T>C
NM_001243133.2(NLRP3):c.-748-307A>G
NM_001243133.2(NLRP3):c.1486G>A (p.Asp496Asn)
NM_001243133.2(NLRP3):c.2151-225C>A
NM_001243133.2(NLRP3):c.2338C>A (p.Leu780Ile)
NM_001243133.2(NLRP3):c.2353T>C (p.Cys785Arg)
NM_001243133.2(NLRP3):c.2835-14C>A
NM_001304359.2(MUC5AC):c.1386+63G>T
NM_001304359.2(MUC5AC):c.14528C>A (p.Thr4843Asn)
NM_001304359.2(MUC5AC):c.14615A>G (p.Glu4872Gly)
NM_001304359.2(MUC5AC):c.15862-71G>T
NM_001304359.2(MUC5AC):c.2093-112C>T
NM_001304359.2(MUC5AC):c.211+43T>C
NM_001304359.2(MUC5AC):c.3777-148T>A
NM_001304359.2(MUC5AC):c.9463A>T (p.Thr3155Ser)
NM_001378902.1(ROS1):c.3167A>G (p.Asn1056Ser)
NM_001378902.1(ROS1):c.5062-46A>C
NM_001378902.1(ROS1):c.682C>G (p.Gln228Glu)
NM_001382430.1(AKT1):c.287+402_287+403delinsGG
NM_002019.4(FLT1):c.1106+219G>T
NM_002019.4(FLT1):c.2594-52G>A
NM_002019.4(FLT1):c.2708-190C>T
NM_002019.4(FLT1):c.2708-195G>T
NM_002019.4(FLT1):c.3174+225T>G
NM_002019.4(FLT1):c.3721-78C>A
NM_002555.6(SLC22A18):c.865-1046C>T
NM_003238.6(TGFB2):c.510+148T>G
NM_004136.4(IREB2):c.1023+1037G>A
NM_004136.4(IREB2):c.1024-1244T>A
NM_004304.5(ALK):c.2205-116G>A
NM_004465.2(FGF10):c.*723C>A
NM_005228.5(EGFR):c.1661A>G (p.Glu554Gly) rs779741928
NM_005228.5(EGFR):c.88+24313G>C
NM_006182.4(DDR2):c.1294-109C>T
NM_006182.4(DDR2):c.1728+293A>G
NM_006982.3(ALX1):c.791G>T (p.Gly264Val)
NM_014491.4(FOXP2):c.1164G>T (p.Val388=)
NM_014491.4(FOXP2):c.2003+1336G>C
NM_014491.4(FOXP2):c.2003+4074C>A
NM_014883.4(FAM13A):c.1459-515_1459-514inv
NM_024832.5(RIN3):c.367+51A>T
NM_024832.5(RIN3):c.44+240_44+241inv
NM_024832.5(RIN3):c.532+232A>C
NM_024832.5(RIN3):c.532+23G>T
NM_033274.5(ADAM19):c.1130+67G>T
NM_033274.5(ADAM19):c.180+659A>C
NM_033274.5(ADAM19):c.251+324T>G
NM_138554.5(TLR4):c.*4092C>T
NM_138554.5(TLR4):c.1431A>T (p.Lys477Asn)
NM_138554.5(TLR4):c.6G>T (p.Met2Ile)
NM_198569.3(ADGRG6):c.2127+438T>C
NM_198569.3(ADGRG6):c.2541+173_2541+175inv
NM_198569.3(ADGRG6):c.2541+185_2541+187delinsTCT
NM_203416.4(CD163):c.3344-144C>G
NM_203416.4(CD163):c.45T>A (p.Ala15=)
NM_207517.3(ADAMTSL3):c.318-243T>C
NM_207517.3(ADAMTSL3):c.4729G>C (p.Asp1577His)

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