ClinVar Miner

List of variants in gene TCF4 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_001083962.2(TCF4):c.1941A>G (p.Ser647=) rs8766 0.37317
NM_001243230.2(TCF4):c.66G>A (p.Glu22=) rs113395332 0.00228
NM_001083962.2(TCF4):c.944C>T (p.Ala315Val) rs147445499 0.00066
NM_001083962.2(TCF4):c.504A>G (p.Val168=) rs370160994 0.00037
NM_001083962.2(TCF4):c.1487-5G>A rs749176054 0.00016
NM_001083962.2(TCF4):c.1545C>T (p.Ser515=) rs777418647 0.00012
NM_001083962.2(TCF4):c.1245T>C (p.His415=) rs148909575 0.00006
NM_001083962.2(TCF4):c.660C>T (p.Gly220=) rs149861305 0.00004
NM_001083962.2(TCF4):c.945C>T (p.Ala315=) rs200115299 0.00004
NM_001083962.2(TCF4):c.1238del (p.Gly413fs)
NM_001083962.2(TCF4):c.1525G>A (p.Gly509Ser)
NM_001083962.2(TCF4):c.1696G>A (p.Glu566Lys)
NM_001083962.2(TCF4):c.1721A>G (p.Asn574Ser) rs796053430
NM_001083962.2(TCF4):c.1727G>A (p.Arg576Gln) rs1057521070
NM_001083962.2(TCF4):c.1733G>A (p.Arg578His) rs121909123
NM_001083962.2(TCF4):c.1763del (p.Phe588fs)
NM_001083962.2(TCF4):c.305-103C>A
NM_001083962.2(TCF4):c.320G>T (p.Gly107Val)
NM_001083962.2(TCF4):c.387T>C (p.Gly129=)
NM_001083962.2(TCF4):c.415C>G (p.Leu139Val)
NM_001083962.2(TCF4):c.537T>A (p.Gly179=)
NM_001083962.2(TCF4):c.550-22790A>G
NM_001083962.2(TCF4):c.633C>G (p.Phe211Leu)
NM_001083962.2(TCF4):c.995A>G (p.Tyr332Cys) rs1568510320
NM_001243226.3(TCF4):c.287-1404G>A

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