ClinVar Miner

List of variants in gene TCF20 reported as uncertain significance by GeneDx

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Gene type:
ClinVar version:
Total variants: 97
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HGVS dbSNP gnomAD frequency
NM_001378418.1(TCF20):c.173G>A (p.Gly58Glu) rs555261601 0.00009
NM_001378418.1(TCF20):c.1705C>T (p.Pro569Ser) rs748165615 0.00002
NM_001378418.1(TCF20):c.2962A>G (p.Met988Val) rs746474528 0.00002
NM_001378418.1(TCF20):c.2566C>T (p.Pro856Ser) rs944264446 0.00001
NM_001378418.1(TCF20):c.2687G>C (p.Arg896Thr) rs1921106705 0.00001
NM_001378418.1(TCF20):c.2695C>T (p.Arg899Cys) rs765753339 0.00001
NM_001378418.1(TCF20):c.5384G>A (p.Cys1795Tyr) rs1920927725 0.00001
NM_001378418.1(TCF20):c.55C>G (p.Gln19Glu) rs1418116716 0.00001
NM_001378418.1(TCF20):c.103_104delinsTA (p.Ala35Tyr)
NM_001378418.1(TCF20):c.1166T>G (p.Leu389Arg)
NM_001378418.1(TCF20):c.1191G>T (p.Gln397His) rs1921392107
NM_001378418.1(TCF20):c.1246C>T (p.Pro416Ser) rs1921384209
NM_001378418.1(TCF20):c.1343T>C (p.Leu448Pro) rs1337121509
NM_001378418.1(TCF20):c.1351C>T (p.Pro451Ser)
NM_001378418.1(TCF20):c.1359G>C (p.Leu453Phe)
NM_001378418.1(TCF20):c.1368G>T (p.Leu456Phe) rs2518236941
NM_001378418.1(TCF20):c.1419G>A (p.Met473Ile)
NM_001378418.1(TCF20):c.1483G>A (p.Ala495Thr)
NM_001378418.1(TCF20):c.1502C>G (p.Ser501Cys)
NM_001378418.1(TCF20):c.1514C>T (p.Ser505Leu)
NM_001378418.1(TCF20):c.1520C>A (p.Pro507His) rs2518235492
NM_001378418.1(TCF20):c.1565G>A (p.Gly522Asp)
NM_001378418.1(TCF20):c.169G>A (p.Gly57Ser) rs1921599592
NM_001378418.1(TCF20):c.1724C>G (p.Pro575Arg) rs751106277
NM_001378418.1(TCF20):c.1766T>C (p.Met589Thr) rs2518233080
NM_001378418.1(TCF20):c.1831G>A (p.Glu611Lys)
NM_001378418.1(TCF20):c.1934A>G (p.Lys645Arg) rs2518231539
NM_001378418.1(TCF20):c.2173C>T (p.Pro725Ser)
NM_001378418.1(TCF20):c.2210C>G (p.Thr737Ser) rs2518228722
NM_001378418.1(TCF20):c.2273A>G (p.Gln758Arg)
NM_001378418.1(TCF20):c.2446C>T (p.His816Tyr) rs2518226258
NM_001378418.1(TCF20):c.2456C>T (p.Pro819Leu)
NM_001378418.1(TCF20):c.2502C>G (p.Ile834Met)
NM_001378418.1(TCF20):c.2552_2553inv (p.Ser851Leu)
NM_001378418.1(TCF20):c.2582C>A (p.Ser861Tyr)
NM_001378418.1(TCF20):c.2669C>A (p.Ala890Asp)
NM_001378418.1(TCF20):c.2704C>T (p.Pro902Ser) rs2518223642
NM_001378418.1(TCF20):c.2774G>A (p.Ser925Asn)
NM_001378418.1(TCF20):c.27T>G (p.Ser9Arg) rs2518250129
NM_001378418.1(TCF20):c.2803C>A (p.Gln935Lys) rs2518222528
NM_001378418.1(TCF20):c.3041A>G (p.Glu1014Gly) rs2147207894
NM_001378418.1(TCF20):c.3103C>G (p.Pro1035Ala)
NM_001378418.1(TCF20):c.3165C>A (p.Asn1055Lys) rs1921012081
NM_001378418.1(TCF20):c.3190_3192del (p.His1064del)
NM_001378418.1(TCF20):c.3211_3212delinsAT (p.Ala1071Ile) rs2518218696
NM_001378418.1(TCF20):c.3223C>T (p.Pro1075Ser)
NM_001378418.1(TCF20):c.3319G>A (p.Gly1107Arg) rs1034640033
NM_001378418.1(TCF20):c.3326T>C (p.Ile1109Thr)
NM_001378418.1(TCF20):c.3397C>G (p.Arg1133Gly) rs756751149
NM_001378418.1(TCF20):c.3401G>C (p.Ser1134Thr) rs2147205823
NM_001378418.1(TCF20):c.3431T>A (p.Met1144Lys)
NM_001378418.1(TCF20):c.3460G>C (p.Asp1154His) rs2518215954
NM_001378418.1(TCF20):c.3491T>C (p.Leu1164Pro) rs1920979533
NM_001378418.1(TCF20):c.3519G>C (p.Lys1173Asn)
NM_001378418.1(TCF20):c.3544C>G (p.Gln1182Glu) rs2147204939
NM_001378418.1(TCF20):c.3633G>T (p.Arg1211Ser) rs758126650
NM_001378418.1(TCF20):c.3670G>C (p.Ala1224Pro)
NM_001378418.1(TCF20):c.3731A>T (p.Asp1244Val) rs2518213022
NM_001378418.1(TCF20):c.3785C>T (p.Ser1262Phe) rs2518212528
NM_001378418.1(TCF20):c.3806A>G (p.Gln1269Arg)
NM_001378418.1(TCF20):c.3893C>T (p.Ser1298Phe) rs1161058665
NM_001378418.1(TCF20):c.3958C>G (p.Leu1320Val) rs774708444
NM_001378418.1(TCF20):c.3986C>G (p.Pro1329Arg) rs776058464
NM_001378418.1(TCF20):c.3995C>A (p.Thr1332Asn) rs1920955579
NM_001378418.1(TCF20):c.4048T>G (p.Leu1350Val)
NM_001378418.1(TCF20):c.4113C>G (p.Asn1371Lys) rs2518209481
NM_001378418.1(TCF20):c.4118C>A (p.Ala1373Glu)
NM_001378418.1(TCF20):c.4171_4173dup (p.Gly1391_Pro1392insGly)
NM_001378418.1(TCF20):c.4204G>A (p.Asp1402Asn) rs2518208719
NM_001378418.1(TCF20):c.429C>G (p.His143Gln) rs1921538757
NM_001378418.1(TCF20):c.4346C>T (p.Thr1449Ile) rs1270397230
NM_001378418.1(TCF20):c.4426C>G (p.Gln1476Glu) rs2147199699
NM_001378418.1(TCF20):c.4468A>G (p.Ile1490Val) rs761145899
NM_001378418.1(TCF20):c.4696A>T (p.Ile1566Leu) rs2518204993
NM_001378418.1(TCF20):c.4742G>A (p.Arg1581Lys)
NM_001378418.1(TCF20):c.4802C>T (p.Ala1601Val)
NM_001378418.1(TCF20):c.4850C>T (p.Ala1617Val) rs2518203686
NM_001378418.1(TCF20):c.4853C>T (p.Thr1618Ile)
NM_001378418.1(TCF20):c.4978T>A (p.Leu1660Ile)
NM_001378418.1(TCF20):c.4997G>A (p.Gly1666Asp) rs1402380311
NM_001378418.1(TCF20):c.5004G>C (p.Arg1668Ser) rs1920932864
NM_001378418.1(TCF20):c.5138G>T (p.Ser1713Ile)
NM_001378418.1(TCF20):c.5176C>T (p.Pro1726Ser) rs2147196163
NM_001378418.1(TCF20):c.5213C>T (p.Pro1738Leu) rs2147195889
NM_001378418.1(TCF20):c.5469C>G (p.Asp1823Glu)
NM_001378418.1(TCF20):c.5633C>T (p.Ala1878Val)
NM_001378418.1(TCF20):c.5676G>C (p.Glu1892Asp) rs2518079856
NM_001378418.1(TCF20):c.5718C>A (p.Phe1906Leu)
NM_001378418.1(TCF20):c.5806C>G (p.Leu1936Val)
NM_001378418.1(TCF20):c.5807T>C (p.Leu1936Pro) rs2518032654
NM_001378418.1(TCF20):c.5825_5826del (p.Pro1942fs) rs756457255
NM_001378418.1(TCF20):c.64C>T (p.His22Tyr) rs1465688329
NM_001378418.1(TCF20):c.725C>G (p.Ser242Cys)
NM_001378418.1(TCF20):c.727_728delinsAT (p.Ser243Ile) rs2518242874
NM_001378418.1(TCF20):c.809C>G (p.Ser270Cys) rs1921471774
NM_001378418.1(TCF20):c.953C>A (p.Pro318Gln)
NM_001378418.1(TCF20):c.960ACA[2] (p.Gln322del) rs552166978

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