ClinVar Miner

List of variants in gene TCF4 reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_001083962.2(TCF4):c.1486+4G>C rs201274415 0.00003
NM_001083962.2(TCF4):c.1349T>C (p.Met450Thr) rs774283982 0.00001
NM_001083962.2(TCF4):c.1412A>G (p.Gln471Arg) rs1285770614 0.00001
NM_001083962.2(TCF4):c.1598A>G (p.Lys533Arg) rs1568329915 0.00001
NM_001083962.2(TCF4):c.649A>T (p.Met217Leu) rs768573052 0.00001
NM_001083962.2(TCF4):c.1061C>G (p.Ser354Cys)
NM_001083962.2(TCF4):c.1070-2A>G
NM_001083962.2(TCF4):c.107G>C (p.Gly36Ala)
NM_001083962.2(TCF4):c.1180G>C (p.Asp394His) rs1198693569
NM_001083962.2(TCF4):c.119T>C (p.Leu40Ser)
NM_001083962.2(TCF4):c.1518CTC[1] (p.Ser508del)
NM_001083962.2(TCF4):c.1628C>T (p.Ser543Leu)
NM_001083962.2(TCF4):c.1942G>C (p.Glu648Gln)
NM_001083962.2(TCF4):c.2003T>G (p.Met668Arg)
NM_001083962.2(TCF4):c.413C>G (p.Thr138Ser) rs796053416
NM_001083962.2(TCF4):c.421C>T (p.Pro141Ser) rs2144786748
NM_001083962.2(TCF4):c.569G>A (p.Ser190Asn)
NM_001083962.2(TCF4):c.579C>G (p.Asp193Glu)
NM_001083962.2(TCF4):c.692G>A (p.Ser231Asn)
NM_001083962.2(TCF4):c.82C>T (p.Pro28Ser)

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