List of variants in gene TCF4 reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001083962.2(TCF4):c.1134del (p.Leu379fs)
NM_001083962.2(TCF4):c.1139del (p.His380fs)	rs2057097206
NM_001083962.2(TCF4):c.1229_1232dup (p.Met411fs)	rs2056308423
NM_001083962.2(TCF4):c.1243_1265dup (p.Gly423fs)
NM_001083962.2(TCF4):c.1739G>A (p.Arg580Gln)	rs121909121
NM_001083962.2(TCF4):c.514_517del (p.Lys172fs)	rs398123561
NM_001083962.2(TCF4):c.520C>T (p.Arg174Ter)	rs878853149
NM_001083962.2(TCF4):c.526del (p.Val176fs)	rs2082085635
NM_001083962.2(TCF4):c.655+2T>G
NM_001083962.2(TCF4):c.665dup (p.His222fs)	rs2061391242

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