List of variants reported as uncertain significance for carcinoma of liver and intrahepatic biliary tract by Fulgent Genetics, Fulgent Genetics

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 97

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HGVS	dbSNP	gnomAD frequency
NM_001127511.3(APC):c.-204A>G	rs554351451	0.00076
NM_000245.4(MET):c.406G>A (p.Val136Ile)	rs199701987	0.00058
NM_000038.6(APC):c.7036C>T (p.Pro2346Ser)	rs200756935	0.00022
NM_000038.6(APC):c.8462A>G (p.Asp2821Gly)	rs780049836	0.00021
NM_000038.6(APC):c.1606G>A (p.Glu536Lys)	rs138098808	0.00015
NM_000038.6(APC):c.5801C>T (p.Pro1934Leu)	rs587780600	0.00012
NM_000245.4(MET):c.2684C>T (p.Thr895Met)	rs199502137	0.00011
NM_006218.4(PIK3CA):c.1130C>G (p.Pro377Arg)	rs113613074	0.00009
NM_000038.6(APC):c.6724A>G (p.Ser2242Gly)	rs201375478	0.00008
NM_000245.4(MET):c.1669A>G (p.Thr557Ala)	rs374733251	0.00008
NM_000038.6(APC):c.8389A>G (p.Ser2797Gly)	rs147287751	0.00007
NM_000245.4(MET):c.1862C>T (p.Thr621Ile)	rs375951814	0.00007
NM_000038.6(APC):c.1193A>G (p.Lys398Arg)	rs145912662	0.00006
NM_000245.4(MET):c.818C>A (p.Thr273Asn)	rs368144654	0.00006
NM_000038.6(APC):c.1553C>T (p.Thr518Met)	rs371453363	0.00005
NM_000038.6(APC):c.4372C>T (p.Pro1458Ser)	rs143796828	0.00005
NM_000038.6(APC):c.1762G>A (p.Val588Ile)	rs372416031	0.00004
NM_000038.6(APC):c.5894A>C (p.His1965Pro)	rs773776516	0.00004
NM_000038.6(APC):c.6639G>A (p.Met2213Ile)	rs35540155	0.00004
NM_000038.6(APC):c.7531C>T (p.Leu2511Phe)	rs72541815	0.00004
NM_000038.6(APC):c.776G>A (p.Arg259Gln)	rs767457050	0.00004
NM_000245.4(MET):c.142G>A (p.Ala48Thr)	rs374050750	0.00004
NM_000245.4(MET):c.4034T>C (p.Ile1345Thr)	rs768188910	0.00004
NM_000546.6(TP53):c.460G>A (p.Gly154Ser)	rs137852789	0.00004
NM_001127511.3(APC):c.-167G>A	rs1278244063	0.00004
NM_000038.6(APC):c.1241G>A (p.Arg414His)	rs730881233	0.00003
NM_000038.6(APC):c.7808A>G (p.Glu2603Gly)	rs587779807	0.00003
NM_000038.6(APC):c.791A>G (p.Gln264Arg)	rs369345931	0.00003
NM_000038.6(APC):c.854A>G (p.Asp285Gly)	rs201093383	0.00003
NM_000245.4(MET):c.2555T>A (p.Met852Lys)	rs369758288	0.00003
NM_000245.4(MET):c.762A>C (p.Glu254Asp)	rs760278126	0.00003
NM_001127511.3(APC):c.-32C>T	rs1015952631	0.00003
NM_001127511.3(APC):c.-88T>G	rs531931776	0.00003
NM_001127511.3(APC):c.1A>G (p.Met1Val)	rs189807660	0.00003
NM_000038.6(APC):c.1538T>C (p.Val513Ala)	rs876658167	0.00002
NM_000038.6(APC):c.3661C>T (p.Pro1221Ser)	rs760999992	0.00002
NM_000038.6(APC):c.4399C>T (p.Pro1467Ser)	rs749142480	0.00002
NM_000038.6(APC):c.5363G>A (p.Arg1788His)	rs201472075	0.00002
NM_000038.6(APC):c.7105C>T (p.Pro2369Ser)	rs377308875	0.00002
NM_000038.6(APC):c.7166G>A (p.Ser2389Asn)	rs779287035	0.00002
NM_000038.6(APC):c.8017A>G (p.Arg2673Gly)	rs767286063	0.00002
NM_000245.4(MET):c.1081G>T (p.Ala361Ser)	rs786202310	0.00002
NM_000245.4(MET):c.4090C>T (p.Pro1364Ser)	rs765332671	0.00002
NM_000546.6(TP53):c.466C>T (p.Arg156Cys)	rs563378859	0.00002
NM_000038.6(APC):c.2114G>A (p.Ser705Asn)	rs752874220	0.00001
NM_000038.6(APC):c.212G>A (p.Arg71His)	rs750503329	0.00001
NM_000038.6(APC):c.2474A>G (p.Tyr825Cys)	rs186641437	0.00001
NM_000038.6(APC):c.3515A>T (p.His1172Leu)	rs1024630299	0.00001
NM_000038.6(APC):c.4430A>G (p.Gln1477Arg)	rs1479009365	0.00001
NM_000038.6(APC):c.4963A>G (p.Thr1655Ala)	rs759441332	0.00001
NM_000038.6(APC):c.5105G>A (p.Gly1702Glu)	rs769273526	0.00001
NM_000038.6(APC):c.5282A>C (p.Asn1761Thr)	rs752038930	0.00001
NM_000038.6(APC):c.5615T>A (p.Val1872Asp)	rs748389037	0.00001
NM_000038.6(APC):c.5627G>T (p.Arg1876Met)	rs773201570	0.00001
NM_000038.6(APC):c.6736G>A (p.Val2246Ile)	rs1055180096	0.00001
NM_000038.6(APC):c.7136C>G (p.Thr2379Ser)	rs767691072	0.00001
NM_000038.6(APC):c.8276G>A (p.Arg2759His)	rs538289470	0.00001
NM_000038.6(APC):c.8282C>T (p.Pro2761Leu)	rs757874563	0.00001
NM_000245.4(MET):c.1336A>G (p.Ile446Val)	rs779022887	0.00001
NM_000245.4(MET):c.143C>G (p.Ala48Gly)	rs80256822	0.00001
NM_000245.4(MET):c.1444G>A (p.Asp482Asn)	rs863224694	0.00001
NM_000245.4(MET):c.446A>G (p.Asn149Ser)	rs772398152	0.00001
NM_000546.6(TP53):c.1000G>C (p.Gly334Arg)	rs730882028	0.00001
NM_000546.6(TP53):c.461G>A (p.Gly154Asp)	rs762846821	0.00001
NM_000546.6(TP53):c.760A>G (p.Ile254Val)	rs746601313	0.00001
NM_006218.4(PIK3CA):c.2651A>G (p.Lys884Arg)	rs1395235750	0.00001
NM_006218.4(PIK3CA):c.436G>A (p.Val146Ile)	rs755969956	0.00001
NM_000038.6(APC):c.1333C>G (p.Gln445Glu)	rs876658802
NM_000038.6(APC):c.2160G>A (p.Met720Ile)	rs1283428855
NM_000038.6(APC):c.2573T>C (p.Ile858Thr)	rs1765215022
NM_000038.6(APC):c.3263A>C (p.Lys1088Thr)	rs1580633119
NM_000038.6(APC):c.3365A>G (p.Asn1122Ser)	rs372855304
NM_000038.6(APC):c.3490A>G (p.Ile1164Val)	rs1554085052
NM_000038.6(APC):c.4332A>T (p.Gln1444His)	rs748342378
NM_000038.6(APC):c.4847A>T (p.Lys1616Ile)	rs1554086241
NM_000038.6(APC):c.4987G>A (p.Glu1663Lys)	rs758987855
NM_000038.6(APC):c.5011G>A (p.Ala1671Thr)	rs587781600
NM_000038.6(APC):c.6218G>A (p.Gly2073Asp)	rs1766164614
NM_000038.6(APC):c.6257C>G (p.Pro2086Arg)	rs786202975
NM_000038.6(APC):c.6727A>G (p.Thr2243Ala)	rs773539706
NM_000038.6(APC):c.7097A>G (p.Tyr2366Cys)	rs1561612604
NM_000038.6(APC):c.7757G>T (p.Ser2586Ile)	rs199806334
NM_000038.6(APC):c.7946C>T (p.Pro2649Leu)	rs1766608503
NM_000038.6(APC):c.813G>A (p.Met271Ile)	rs1064793903
NM_000038.6(APC):c.8281C>T (p.Pro2761Ser)	rs1060503332
NM_000245.4(MET):c.1157T>G (p.Leu386Arg)	rs1554379180
NM_000245.4(MET):c.1174C>A (p.Pro392Thr)	rs886061943
NM_000245.4(MET):c.1933G>A (p.Gly645Arg)	rs763849125
NM_000245.4(MET):c.2191C>T (p.Arg731Ter)	rs377336878
NM_000245.4(MET):c.2375A>G (p.His792Arg)	rs980467681
NM_000245.4(MET):c.2893G>A (p.Gly965Ser)	rs1413209214
NM_000245.4(MET):c.4122C>A (p.Asn1374Lys)	rs370767911
NM_000245.4(MET):c.799G>A (p.Glu267Lys)	rs755954919
NM_000546.6(TP53):c.677G>C (p.Gly226Ala)	rs970212462
NM_001127511.3(APC):c.-128G>C	rs543098847
NM_001127511.3(APC):c.-142G>A	rs951500465
NM_001904.4(CTNNB1):c.1571A>G (p.His524Arg)	rs1376864427

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