ClinVar Miner

List of variants in gene TCF20 studied for Inborn genetic diseases

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 188
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001378418.1(TCF20):c.1216G>A (p.Gly406Ser) rs143327169 0.00101
NM_001378418.1(TCF20):c.5491A>G (p.Thr1831Ala) rs145292779 0.00047
NM_001378418.1(TCF20):c.5234T>C (p.Met1745Thr) rs137887011 0.00032
NM_001378418.1(TCF20):c.73T>G (p.Ser25Ala) rs116800891 0.00032
NM_001378418.1(TCF20):c.2149G>A (p.Val717Met) rs150138145 0.00031
NM_001378418.1(TCF20):c.232_234dup (p.Gly78_Tyr79insGly) rs751529766 0.00031
NM_001378418.1(TCF20):c.1029A>C (p.Gln343His) rs150925429 0.00026
NM_001378418.1(TCF20):c.1846C>T (p.Arg616Trp) rs148999987 0.00017
NM_001378418.1(TCF20):c.3254A>G (p.Tyr1085Cys) rs200659809 0.00011
NM_001378418.1(TCF20):c.5407T>G (p.Ser1803Ala) rs375600166 0.00011
NM_001378418.1(TCF20):c.173G>A (p.Gly58Glu) rs555261601 0.00009
NM_001378418.1(TCF20):c.2120A>G (p.Tyr707Cys) rs764736571 0.00009
NM_001378418.1(TCF20):c.3478G>A (p.Ala1160Thr) rs373813794 0.00009
NM_001378418.1(TCF20):c.3589C>T (p.Pro1197Ser) rs144735319 0.00009
NM_001378418.1(TCF20):c.3874G>A (p.Ala1292Thr) rs775825597 0.00009
NM_001378418.1(TCF20):c.5201C>T (p.Pro1734Leu) rs767396058 0.00009
NM_001378418.1(TCF20):c.199G>T (p.Ala67Ser) rs202014904 0.00007
NM_001378418.1(TCF20):c.442G>A (p.Gly148Ser) rs143676414 0.00007
NM_001378418.1(TCF20):c.284A>G (p.Asn95Ser) rs771822478 0.00006
NM_001378418.1(TCF20):c.4291C>G (p.Pro1431Ala) rs200904088 0.00006
NM_001378418.1(TCF20):c.4369G>A (p.Gly1457Arg) rs761096672 0.00006
NM_001378418.1(TCF20):c.4393A>G (p.Thr1465Ala) rs377612395 0.00006
NM_001378418.1(TCF20):c.1394A>G (p.Asn465Ser) rs776191510 0.00005
NM_001378418.1(TCF20):c.1729G>A (p.Ala577Thr) rs538252151 0.00005
NM_001378418.1(TCF20):c.2645C>T (p.Ala882Val) rs778749289 0.00005
NM_001378418.1(TCF20):c.2957C>T (p.Thr986Met) rs780984632 0.00005
NM_001378418.1(TCF20):c.3230C>T (p.Ala1077Val) rs570476985 0.00005
NM_001378418.1(TCF20):c.3718C>G (p.Pro1240Ala) rs768771719 0.00005
NM_001378418.1(TCF20):c.3877G>C (p.Asp1293His) rs374767438 0.00005
NM_001378418.1(TCF20):c.3943G>A (p.Asp1315Asn) rs929676419 0.00005
NM_001378418.1(TCF20):c.1186C>A (p.Leu396Ile) rs370003646 0.00004
NM_001378418.1(TCF20):c.2738G>A (p.Gly913Asp) rs141527051 0.00004
NM_001378418.1(TCF20):c.4681C>G (p.Pro1561Ala) rs780455998 0.00004
NM_001378418.1(TCF20):c.1270A>G (p.Met424Val) rs762875633 0.00003
NM_001378418.1(TCF20):c.2332A>G (p.Met778Val) rs777773135 0.00003
NM_001378418.1(TCF20):c.2483C>T (p.Ala828Val) rs560419170 0.00003
NM_001378418.1(TCF20):c.2825T>A (p.Phe942Tyr) rs377143209 0.00003
NM_001378418.1(TCF20):c.2887G>A (p.Gly963Ser) rs200854743 0.00003
NM_001378418.1(TCF20):c.3604G>A (p.Gly1202Ser) rs149389913 0.00003
NM_001378418.1(TCF20):c.4312C>T (p.Arg1438Cys) rs771336001 0.00003
NM_001378418.1(TCF20):c.4313G>A (p.Arg1438His) rs149724958 0.00003
NM_001378418.1(TCF20):c.4922G>A (p.Cys1641Tyr) rs1396989717 0.00003
NM_001378418.1(TCF20):c.5093C>T (p.Ser1698Leu) rs554899790 0.00003
NM_001378418.1(TCF20):c.5144G>A (p.Arg1715Gln) rs765119165 0.00003
NM_001378418.1(TCF20):c.5757G>T (p.Leu1919Phe) rs371117943 0.00003
NM_001378418.1(TCF20):c.1715A>G (p.Asn572Ser) rs574867061 0.00002
NM_001378418.1(TCF20):c.1873A>G (p.Lys625Glu) rs1373543403 0.00002
NM_001378418.1(TCF20):c.2399G>A (p.Ser800Asn) rs1033585471 0.00002
NM_001378418.1(TCF20):c.3622A>G (p.Ser1208Gly) rs200272467 0.00002
NM_001378418.1(TCF20):c.3848G>A (p.Arg1283His) rs750743110 0.00002
NM_001378418.1(TCF20):c.4016C>T (p.Thr1339Ile) rs1920954953 0.00002
NM_001378418.1(TCF20):c.5024G>C (p.Ser1675Thr) rs142975381 0.00002
NM_001378418.1(TCF20):c.5446A>G (p.Ser1816Gly) rs531202529 0.00002
NM_001378418.1(TCF20):c.94C>T (p.Pro32Ser) rs775736964 0.00002
NM_001378418.1(TCF20):c.1283C>T (p.Pro428Leu) rs1202079826 0.00001
NM_001378418.1(TCF20):c.1787A>G (p.Asn596Ser) rs757979794 0.00001
NM_001378418.1(TCF20):c.1844G>T (p.Gly615Val) rs766549069 0.00001
NM_001378418.1(TCF20):c.1857G>T (p.Lys619Asn) rs768461101 0.00001
NM_001378418.1(TCF20):c.1922A>G (p.Asn641Ser) rs547085733 0.00001
NM_001378418.1(TCF20):c.2062G>A (p.Ala688Thr) rs755315170 0.00001
NM_001378418.1(TCF20):c.2078C>T (p.Thr693Met) rs750513879 0.00001
NM_001378418.1(TCF20):c.2140G>A (p.Gly714Arg) rs772874257 0.00001
NM_001378418.1(TCF20):c.2156G>A (p.Arg719Gln) rs746307234 0.00001
NM_001378418.1(TCF20):c.220T>C (p.Ser74Pro) rs1205483259 0.00001
NM_001378418.1(TCF20):c.221C>G (p.Ser74Cys) rs1921581987 0.00001
NM_001378418.1(TCF20):c.2420G>A (p.Ser807Asn) rs1291798813 0.00001
NM_001378418.1(TCF20):c.2744T>G (p.Val915Gly) rs200895127 0.00001
NM_001378418.1(TCF20):c.2857C>A (p.Pro953Thr) rs1921074516 0.00001
NM_001378418.1(TCF20):c.2918A>T (p.Asp973Val) rs774763275 0.00001
NM_001378418.1(TCF20):c.2974C>T (p.Pro992Ser) rs369800379 0.00001
NM_001378418.1(TCF20):c.3121G>C (p.Glu1041Gln) rs1450225029 0.00001
NM_001378418.1(TCF20):c.331C>T (p.Pro111Ser) rs1172143599 0.00001
NM_001378418.1(TCF20):c.3536A>G (p.His1179Arg) rs749962037 0.00001
NM_001378418.1(TCF20):c.362C>A (p.Pro121His) rs1250624367 0.00001
NM_001378418.1(TCF20):c.3643C>T (p.Pro1215Ser) rs778975222 0.00001
NM_001378418.1(TCF20):c.3677C>G (p.Ala1226Gly) rs1269982549 0.00001
NM_001378418.1(TCF20):c.3781A>C (p.Ile1261Leu) rs770945649 0.00001
NM_001378418.1(TCF20):c.383A>G (p.Asn128Ser) rs748499160 0.00001
NM_001378418.1(TCF20):c.3847C>A (p.Arg1283Ser) rs138491277 0.00001
NM_001378418.1(TCF20):c.3916C>G (p.Gln1306Glu) rs780925899 0.00001
NM_001378418.1(TCF20):c.3931A>G (p.Ile1311Val) rs367931028 0.00001
NM_001378418.1(TCF20):c.4109C>T (p.Ser1370Leu) rs768208107 0.00001
NM_001378418.1(TCF20):c.4272G>T (p.Leu1424Phe) rs1262297897 0.00001
NM_001378418.1(TCF20):c.4282A>G (p.Lys1428Glu) rs1920946515 0.00001
NM_001378418.1(TCF20):c.4519G>A (p.Ala1507Thr) rs780973217 0.00001
NM_001378418.1(TCF20):c.4778C>T (p.Pro1593Leu) rs745858743 0.00001
NM_001378418.1(TCF20):c.4903A>G (p.Ile1635Val) rs368604405 0.00001
NM_001378418.1(TCF20):c.5036G>C (p.Ser1679Thr) rs762862108 0.00001
NM_001378418.1(TCF20):c.5257C>T (p.His1753Tyr) rs765172300 0.00001
NM_001378418.1(TCF20):c.52C>T (p.Pro18Ser) rs780657916 0.00001
NM_001378418.1(TCF20):c.5360A>G (p.Lys1787Arg) rs1920928065 0.00001
NM_001378418.1(TCF20):c.5375C>T (p.Ser1792Leu) rs373214954 0.00001
NM_001378418.1(TCF20):c.5451T>G (p.Ser1817Arg) rs1920926710 0.00001
NM_001378418.1(TCF20):c.5549A>G (p.Asn1850Ser) rs780958269 0.00001
NM_001378418.1(TCF20):c.5818C>G (p.Leu1940Val) rs766229168 0.00001
NM_001378418.1(TCF20):c.659C>T (p.Ser220Phe) rs186320252 0.00001
NM_001378418.1(TCF20):c.827A>G (p.Asn276Ser) rs758391601 0.00001
NM_001378418.1(TCF20):c.1327G>A (p.Val443Ile) rs2518237405
NM_001378418.1(TCF20):c.14G>T (p.Arg5Leu)
NM_001378418.1(TCF20):c.1551G>C (p.Glu517Asp)
NM_001378418.1(TCF20):c.1591G>A (p.Gly531Ser) rs1921315787
NM_001378418.1(TCF20):c.1603C>T (p.Arg535Trp)
NM_001378418.1(TCF20):c.1664A>G (p.Lys555Arg)
NM_001378418.1(TCF20):c.1666G>A (p.Ala556Thr) rs777016897
NM_001378418.1(TCF20):c.1744A>G (p.Thr582Ala) rs376787114
NM_001378418.1(TCF20):c.1780G>A (p.Asp594Asn) rs375607848
NM_001378418.1(TCF20):c.1806G>T (p.Lys602Asn)
NM_001378418.1(TCF20):c.181G>C (p.Gly61Arg) rs751875361
NM_001378418.1(TCF20):c.1874A>G (p.Lys625Arg) rs1175452016
NM_001378418.1(TCF20):c.1984G>T (p.Gly662Trp)
NM_001378418.1(TCF20):c.1994G>T (p.Gly665Val)
NM_001378418.1(TCF20):c.2066G>A (p.Gly689Asp) rs1034050418
NM_001378418.1(TCF20):c.2221G>C (p.Glu741Gln)
NM_001378418.1(TCF20):c.2224C>T (p.Arg742Ter) rs1555926209
NM_001378418.1(TCF20):c.232G>C (p.Gly78Arg)
NM_001378418.1(TCF20):c.2380C>G (p.Gln794Glu) rs1179947634
NM_001378418.1(TCF20):c.2413A>T (p.Asn805Tyr) rs772770027
NM_001378418.1(TCF20):c.2415C>G (p.Asn805Lys)
NM_001378418.1(TCF20):c.2460G>C (p.Trp820Cys) rs893524266
NM_001378418.1(TCF20):c.2472_2486dup (p.Pro829_Glu830insSerSerThrAlaPro) rs1921146718
NM_001378418.1(TCF20):c.2497C>G (p.Gln833Glu)
NM_001378418.1(TCF20):c.2558C>G (p.Ala853Gly) rs1921131955
NM_001378418.1(TCF20):c.259G>A (p.Gly87Arg)
NM_001378418.1(TCF20):c.2638C>G (p.Pro880Ala)
NM_001378418.1(TCF20):c.2685del (p.Arg896fs) rs1555925903
NM_001378418.1(TCF20):c.2707A>G (p.Thr903Ala) rs1314212425
NM_001378418.1(TCF20):c.275T>C (p.Met92Thr)
NM_001378418.1(TCF20):c.276G>A (p.Met92Ile)
NM_001378418.1(TCF20):c.2786_2787del (p.Lys929fs) rs1921088321
NM_001378418.1(TCF20):c.2804A>G (p.Gln935Arg)
NM_001378418.1(TCF20):c.2860C>G (p.Pro954Ala)
NM_001378418.1(TCF20):c.295G>A (p.Val99Met)
NM_001378418.1(TCF20):c.298A>G (p.Thr100Ala)
NM_001378418.1(TCF20):c.3001A>G (p.Met1001Val)
NM_001378418.1(TCF20):c.3005G>A (p.Arg1002Lys) rs2147208130
NM_001378418.1(TCF20):c.3017C>T (p.Pro1006Leu) rs1483366690
NM_001378418.1(TCF20):c.3053T>C (p.Met1018Thr)
NM_001378418.1(TCF20):c.3194C>G (p.Ala1065Gly)
NM_001378418.1(TCF20):c.3202C>T (p.Arg1068Trp)
NM_001378418.1(TCF20):c.32A>G (p.His11Arg) rs770746460
NM_001378418.1(TCF20):c.3310T>C (p.Ser1104Pro)
NM_001378418.1(TCF20):c.3322G>A (p.Val1108Ile)
NM_001378418.1(TCF20):c.3670G>A (p.Ala1224Thr)
NM_001378418.1(TCF20):c.383A>T (p.Asn128Ile) rs748499160
NM_001378418.1(TCF20):c.3883G>A (p.Ala1295Thr)
NM_001378418.1(TCF20):c.3932T>C (p.Ile1311Thr) rs2518211047
NM_001378418.1(TCF20):c.3980A>G (p.Asn1327Ser) rs2518210476
NM_001378418.1(TCF20):c.4087A>G (p.Asn1363Asp) rs1481673758
NM_001378418.1(TCF20):c.4129G>A (p.Gly1377Arg) rs2518209326
NM_001378418.1(TCF20):c.418C>A (p.Gln140Lys) rs757449902
NM_001378418.1(TCF20):c.4198G>T (p.Val1400Phe)
NM_001378418.1(TCF20):c.4285C>T (p.Pro1429Ser)
NM_001378418.1(TCF20):c.4291C>T (p.Pro1431Ser) rs200904088
NM_001378418.1(TCF20):c.4321G>A (p.Val1441Met) rs147643985
NM_001378418.1(TCF20):c.4330A>G (p.Lys1444Glu) rs1920945135
NM_001378418.1(TCF20):c.4364C>T (p.Thr1455Ile)
NM_001378418.1(TCF20):c.4368del (p.Gly1457fs) rs1555924435
NM_001378418.1(TCF20):c.4377A>C (p.Glu1459Asp)
NM_001378418.1(TCF20):c.4379C>T (p.Pro1460Leu)
NM_001378418.1(TCF20):c.4382C>G (p.Pro1461Arg)
NM_001378418.1(TCF20):c.4463C>G (p.Pro1488Arg)
NM_001378418.1(TCF20):c.4547_4558del (p.Asn1516_Val1519del) rs1569144688
NM_001378418.1(TCF20):c.4811T>C (p.Ile1604Thr) rs1457495332
NM_001378418.1(TCF20):c.4978T>A (p.Leu1660Ile)
NM_001378418.1(TCF20):c.5069dup (p.Pro1692fs) rs1555923822
NM_001378418.1(TCF20):c.5149A>G (p.Met1717Val)
NM_001378418.1(TCF20):c.5255G>A (p.Arg1752Gln)
NM_001378418.1(TCF20):c.5263A>G (p.Ser1755Gly) rs987449243
NM_001378418.1(TCF20):c.5290A>G (p.Thr1764Ala)
NM_001378418.1(TCF20):c.5308CAG[6] (p.Gln1774dup) rs745763431
NM_001378418.1(TCF20):c.5323A>G (p.Lys1775Glu) rs768655264
NM_001378418.1(TCF20):c.5328G>T (p.Glu1776Asp) rs376915153
NM_001378418.1(TCF20):c.538G>A (p.Val180Ile) rs1217832762
NM_001378418.1(TCF20):c.5395C>G (p.Pro1799Ala) rs765741807
NM_001378418.1(TCF20):c.5641A>G (p.Ile1881Val)
NM_001378418.1(TCF20):c.5651A>T (p.Glu1884Val)
NM_001378418.1(TCF20):c.5719del (p.Arg1907fs) rs1936673622
NM_001378418.1(TCF20):c.5753G>C (p.Cys1918Ser) rs2518037704
NM_001378418.1(TCF20):c.5824C>T (p.Pro1942Ser) rs115095004
NM_001378418.1(TCF20):c.5842G>A (p.Ala1948Thr) rs539500058
NM_001378418.1(TCF20):c.5842G>T (p.Ala1948Ser) rs539500058
NM_001378418.1(TCF20):c.5875C>T (p.Arg1959Trp)
NM_001378418.1(TCF20):c.5876G>A (p.Arg1959Gln) rs763374542
NM_001378418.1(TCF20):c.647C>T (p.Thr216Ile) rs2518243542
NM_001378418.1(TCF20):c.737C>T (p.Ser246Phe)
NM_001378418.1(TCF20):c.7T>C (p.Ser3Pro) rs2518250283
NM_001378418.1(TCF20):c.919C>T (p.Gln307Ter)
NM_001378418.1(TCF20):c.992A>G (p.Tyr331Cys) rs1386615321

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.