ClinVar Miner

List of variants in gene TCF20 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 89
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HGVS dbSNP gnomAD frequency
NM_001378418.1(TCF20):c.5055G>A (p.Ser1685=) rs2070116 0.21810
NM_001378418.1(TCF20):c.2164A>G (p.Ser722Gly) rs5758651 0.17735
NM_001378418.1(TCF20):c.1213A>G (p.Met405Val) rs34030679 0.09205
NM_001378418.1(TCF20):c.138C>T (p.Gly46=) rs61745937 0.03202
NM_001378418.1(TCF20):c.3495G>A (p.Met1165Ile) rs17002890 0.03179
NM_001378418.1(TCF20):c.3974G>A (p.Ser1325Asn) rs17002888 0.01939
NM_001378418.1(TCF20):c.519C>T (p.Ser173=) rs142871472 0.01304
NM_001378418.1(TCF20):c.441C>T (p.Gly147=) rs73887968 0.01026
NM_001378418.1(TCF20):c.47G>C (p.Ser16Thr) rs143525991 0.00959
NM_001378418.1(TCF20):c.204G>A (p.Ala68=) rs146936937 0.00883
NM_001378418.1(TCF20):c.1467C>T (p.Pro489=) rs78356795 0.00684
NM_001378418.1(TCF20):c.354T>C (p.Tyr118=) rs34161538 0.00581
NM_001378418.1(TCF20):c.4241C>T (p.Ser1414Leu) rs145553394 0.00367
NM_001378418.1(TCF20):c.5656-11C>T rs181020107 0.00312
NM_001378418.1(TCF20):c.4407A>G (p.Ser1469=) rs140619869 0.00280
NM_001378418.1(TCF20):c.1056T>C (p.Val352=) rs142522528 0.00246
NM_001378418.1(TCF20):c.4670C>T (p.Pro1557Leu) rs199838890 0.00183
NM_001378418.1(TCF20):c.197C>T (p.Ala66Val) rs137863794 0.00132
NM_001378418.1(TCF20):c.5799+18A>G rs117428927 0.00067
NM_001378418.1(TCF20):c.5491A>G (p.Thr1831Ala) rs145292779 0.00047
NM_001378418.1(TCF20):c.5800-8C>T rs183282164 0.00039
NM_001378418.1(TCF20):c.4119G>A (p.Ala1373=) rs533790420 0.00037
NM_001378418.1(TCF20):c.4320C>T (p.Ser1440=) rs142237336 0.00037
NM_001378418.1(TCF20):c.1845T>C (p.Gly615=) rs147095399 0.00036
NM_001378418.1(TCF20):c.1029A>C (p.Gln343His) rs150925429 0.00026
NM_001378418.1(TCF20):c.191C>T (p.Ala64Val) rs199530245 0.00014
NM_001378418.1(TCF20):c.2797T>C (p.Phe933Leu) rs201923234 0.00010
NM_001378418.1(TCF20):c.442G>A (p.Gly148Ser) rs143676414 0.00007
NM_001378418.1(TCF20):c.148_153del (p.Ser50_Ser51del) rs760555989 0.00005
NM_001378418.1(TCF20):c.2661C>T (p.His887=) rs201660335 0.00004
NM_001378418.1(TCF20):c.4681C>G (p.Pro1561Ala) rs780455998 0.00004
NM_001378418.1(TCF20):c.2887G>A (p.Gly963Ser) rs200854743 0.00003
NM_001378418.1(TCF20):c.4815G>A (p.Val1605=) rs201624158 0.00003
NM_001378418.1(TCF20):c.1340G>A (p.Arg447Gln)
NM_001378418.1(TCF20):c.1440T>G (p.Thr480=) rs17002894
NM_001378418.1(TCF20):c.150CAGTGG[2] (p.51SG[2]) rs541147459
NM_001378418.1(TCF20):c.1715A>G (p.Asn572Ser)
NM_001378418.1(TCF20):c.1787A>G (p.Asn596Ser)
NM_001378418.1(TCF20):c.219C>T (p.Thr73=)
NM_001378418.1(TCF20):c.2265A>G (p.Glu755=)
NM_001378418.1(TCF20):c.232_234dup (p.Gly78_Tyr79insGly)
NM_001378418.1(TCF20):c.2427G>T (p.Gly809=)
NM_001378418.1(TCF20):c.2580C>G (p.Leu860=) rs147254163
NM_001378418.1(TCF20):c.2619A>C (p.Leu873=)
NM_001378418.1(TCF20):c.2673C>A (p.Asp891Glu)
NM_001378418.1(TCF20):c.2681T>C (p.Ile894Thr)
NM_001378418.1(TCF20):c.284A>G (p.Asn95Ser)
NM_001378418.1(TCF20):c.2974C>G (p.Pro992Ala)
NM_001378418.1(TCF20):c.3228C>T (p.Asn1076=)
NM_001378418.1(TCF20):c.3462C>T (p.Asp1154=)
NM_001378418.1(TCF20):c.3643C>T (p.Pro1215Ser)
NM_001378418.1(TCF20):c.3647A>G (p.His1216Arg)
NM_001378418.1(TCF20):c.3660A>T (p.Gly1220=)
NM_001378418.1(TCF20):c.3668T>A (p.Leu1223Gln)
NM_001378418.1(TCF20):c.3701G>A (p.Ser1234Asn)
NM_001378418.1(TCF20):c.383A>G (p.Asn128Ser)
NM_001378418.1(TCF20):c.3874G>A (p.Ala1292Thr)
NM_001378418.1(TCF20):c.3917A>G (p.Gln1306Arg)
NM_001378418.1(TCF20):c.4003A>G (p.Ser1335Gly)
NM_001378418.1(TCF20):c.401G>A (p.Gly134Asp)
NM_001378418.1(TCF20):c.4291C>G (p.Pro1431Ala)
NM_001378418.1(TCF20):c.4294A>G (p.Arg1432Gly)
NM_001378418.1(TCF20):c.4387G>A (p.Ala1463Thr)
NM_001378418.1(TCF20):c.4431G>A (p.Gly1477=)
NM_001378418.1(TCF20):c.4494T>C (p.Pro1498=)
NM_001378418.1(TCF20):c.4569G>A (p.Pro1523=)
NM_001378418.1(TCF20):c.4770G>A (p.Gly1590=)
NM_001378418.1(TCF20):c.4902C>T (p.Tyr1634=)
NM_001378418.1(TCF20):c.5049G>A (p.Pro1683=)
NM_001378418.1(TCF20):c.5093C>T (p.Ser1698Leu)
NM_001378418.1(TCF20):c.5277C>T (p.Gly1759=)
NM_001378418.1(TCF20):c.5372G>A (p.Arg1791His)
NM_001378418.1(TCF20):c.5407T>G (p.Ser1803Ala)
NM_001378418.1(TCF20):c.5442G>A (p.Glu1814=)
NM_001378418.1(TCF20):c.5450G>A (p.Ser1817Asn)
NM_001378418.1(TCF20):c.5526C>T (p.Ile1842=)
NM_001378418.1(TCF20):c.5682C>T (p.Gly1894=)
NM_001378418.1(TCF20):c.5810C>T (p.Pro1937Leu)
NM_001378418.1(TCF20):c.5818C>G (p.Leu1940Val)
NM_001378418.1(TCF20):c.5824C>A (p.Pro1942Thr)
NM_001378418.1(TCF20):c.5824C>G (p.Pro1942Ala)
NM_001378418.1(TCF20):c.5824C>T (p.Pro1942Ser)
NM_001378418.1(TCF20):c.5825C>A (p.Pro1942His) rs144341537
NM_001378418.1(TCF20):c.5825C>G (p.Pro1942Arg)
NM_001378418.1(TCF20):c.5857A>T (p.Ser1953Cys)
NM_001378418.1(TCF20):c.62T>C (p.Val21Ala)
NM_001378418.1(TCF20):c.719CCT[8] (p.Ser246dup) rs754279263
NM_001378418.1(TCF20):c.960ACA[2] (p.Gln322del)
NM_001378418.1(TCF20):c.999C>T (p.Asn333=)

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