ClinVar Miner

List of variants in gene TCF20 reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 90
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HGVS dbSNP gnomAD frequency
NM_001378418.1(TCF20):c.2149G>A (p.Val717Met) rs150138145 0.00031
NM_001378418.1(TCF20):c.4369G>A (p.Gly1457Arg) rs761096672 0.00006
NM_001378418.1(TCF20):c.3718C>G (p.Pro1240Ala) rs768771719 0.00004
NM_001378418.1(TCF20):c.4681C>G (p.Pro1561Ala) rs780455998 0.00004
NM_001378418.1(TCF20):c.2825T>A (p.Phe942Tyr) rs377143209 0.00003
NM_001378418.1(TCF20):c.5757G>T (p.Leu1919Phe) rs371117943 0.00003
NM_001378418.1(TCF20):c.2918A>T (p.Asp973Val) rs774763275 0.00001
NM_001378418.1(TCF20):c.5549A>G (p.Asn1850Ser) rs780958269 0.00001
NM_001378418.1(TCF20):c.1186C>A (p.Leu396Ile)
NM_001378418.1(TCF20):c.1270A>G (p.Met424Val)
NM_001378418.1(TCF20):c.1327G>A (p.Val443Ile)
NM_001378418.1(TCF20):c.1394A>G (p.Asn465Ser)
NM_001378418.1(TCF20):c.1666G>A (p.Ala556Thr)
NM_001378418.1(TCF20):c.1715A>G (p.Asn572Ser)
NM_001378418.1(TCF20):c.1729G>A (p.Ala577Thr)
NM_001378418.1(TCF20):c.1744A>G (p.Thr582Ala)
NM_001378418.1(TCF20):c.1780G>A (p.Asp594Asn)
NM_001378418.1(TCF20):c.1787A>G (p.Asn596Ser)
NM_001378418.1(TCF20):c.181G>C (p.Gly61Arg)
NM_001378418.1(TCF20):c.1844G>T (p.Gly615Val)
NM_001378418.1(TCF20):c.1846C>T (p.Arg616Trp)
NM_001378418.1(TCF20):c.1857G>T (p.Lys619Asn)
NM_001378418.1(TCF20):c.1873A>G (p.Lys625Glu)
NM_001378418.1(TCF20):c.1922A>G (p.Asn641Ser)
NM_001378418.1(TCF20):c.199G>T (p.Ala67Ser)
NM_001378418.1(TCF20):c.220T>C (p.Ser74Pro)
NM_001378418.1(TCF20):c.221C>G (p.Ser74Cys) rs1921581987
NM_001378418.1(TCF20):c.2224C>T (p.Arg742Ter) rs1555926209
NM_001378418.1(TCF20):c.2332A>G (p.Met778Val)
NM_001378418.1(TCF20):c.2380C>G (p.Gln794Glu)
NM_001378418.1(TCF20):c.2413A>T (p.Asn805Tyr)
NM_001378418.1(TCF20):c.2420G>A (p.Ser807Asn)
NM_001378418.1(TCF20):c.2460G>C (p.Trp820Cys)
NM_001378418.1(TCF20):c.2558C>G (p.Ala853Gly)
NM_001378418.1(TCF20):c.2645C>T (p.Ala882Val)
NM_001378418.1(TCF20):c.2685del (p.Arg896fs) rs1555925903
NM_001378418.1(TCF20):c.2707A>G (p.Thr903Ala) rs1314212425
NM_001378418.1(TCF20):c.2738G>A (p.Gly913Asp)
NM_001378418.1(TCF20):c.2744T>G (p.Val915Gly)
NM_001378418.1(TCF20):c.2786_2787del (p.Lys929fs) rs1921088321
NM_001378418.1(TCF20):c.284A>G (p.Asn95Ser)
NM_001378418.1(TCF20):c.2974C>T (p.Pro992Ser)
NM_001378418.1(TCF20):c.3017C>T (p.Pro1006Leu)
NM_001378418.1(TCF20):c.3254A>G (p.Tyr1085Cys)
NM_001378418.1(TCF20):c.3536A>G (p.His1179Arg)
NM_001378418.1(TCF20):c.3589C>T (p.Pro1197Ser)
NM_001378418.1(TCF20):c.3604G>A (p.Gly1202Ser)
NM_001378418.1(TCF20):c.3677C>G (p.Ala1226Gly) rs1269982549
NM_001378418.1(TCF20):c.3781A>C (p.Ile1261Leu)
NM_001378418.1(TCF20):c.383A>G (p.Asn128Ser)
NM_001378418.1(TCF20):c.383A>T (p.Asn128Ile)
NM_001378418.1(TCF20):c.3847C>A (p.Arg1283Ser)
NM_001378418.1(TCF20):c.3916C>G (p.Gln1306Glu)
NM_001378418.1(TCF20):c.3931A>G (p.Ile1311Val)
NM_001378418.1(TCF20):c.4109C>T (p.Ser1370Leu)
NM_001378418.1(TCF20):c.4129G>A (p.Gly1377Arg)
NM_001378418.1(TCF20):c.418C>A (p.Gln140Lys)
NM_001378418.1(TCF20):c.4291C>T (p.Pro1431Ser)
NM_001378418.1(TCF20):c.4321G>A (p.Val1441Met)
NM_001378418.1(TCF20):c.4368del (p.Gly1457fs) rs1555924435
NM_001378418.1(TCF20):c.4519G>A (p.Ala1507Thr)
NM_001378418.1(TCF20):c.4547_4558del (p.Asn1516_Val1519del)
NM_001378418.1(TCF20):c.4778C>T (p.Pro1593Leu)
NM_001378418.1(TCF20):c.4811T>C (p.Ile1604Thr)
NM_001378418.1(TCF20):c.4922G>A (p.Cys1641Tyr)
NM_001378418.1(TCF20):c.5024G>C (p.Ser1675Thr)
NM_001378418.1(TCF20):c.5036G>C (p.Ser1679Thr)
NM_001378418.1(TCF20):c.5069dup (p.Pro1692fs) rs1555923822
NM_001378418.1(TCF20):c.5234T>C (p.Met1745Thr)
NM_001378418.1(TCF20):c.5257C>T (p.His1753Tyr)
NM_001378418.1(TCF20):c.5263A>G (p.Ser1755Gly)
NM_001378418.1(TCF20):c.52C>T (p.Pro18Ser)
NM_001378418.1(TCF20):c.5328G>T (p.Glu1776Asp) rs376915153
NM_001378418.1(TCF20):c.5360A>G (p.Lys1787Arg)
NM_001378418.1(TCF20):c.5375C>T (p.Ser1792Leu)
NM_001378418.1(TCF20):c.538G>A (p.Val180Ile)
NM_001378418.1(TCF20):c.5395C>G (p.Pro1799Ala)
NM_001378418.1(TCF20):c.5446A>G (p.Ser1816Gly)
NM_001378418.1(TCF20):c.5719del (p.Arg1907fs) rs1936673622
NM_001378418.1(TCF20):c.5753G>C (p.Cys1918Ser)
NM_001378418.1(TCF20):c.5818C>G (p.Leu1940Val)
NM_001378418.1(TCF20):c.5842G>T (p.Ala1948Ser)
NM_001378418.1(TCF20):c.5876G>A (p.Arg1959Gln)
NM_001378418.1(TCF20):c.647C>T (p.Thr216Ile)
NM_001378418.1(TCF20):c.659C>T (p.Ser220Phe)
NM_001378418.1(TCF20):c.73T>G (p.Ser25Ala)
NM_001378418.1(TCF20):c.7T>C (p.Ser3Pro)
NM_001378418.1(TCF20):c.827A>G (p.Asn276Ser)
NM_001378418.1(TCF20):c.94C>T (p.Pro32Ser)
NM_001378418.1(TCF20):c.992A>G (p.Tyr331Cys)

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