List of variants in gene TCF4 reported as uncertain significance 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001083962.2(TCF4):c.573T>C (p.Thr191=)	rs1434749460	0.00001
NM_001083962.2(TCF4):c.946G>A (p.Gly316Ser)	rs993457884	0.00001
NM_001083962.2(TCF4):c.1057C>A (p.Pro353Thr)
NM_001083962.2(TCF4):c.1196T>C (p.Val399Ala)	rs2145502188
NM_001083962.2(TCF4):c.146-46442G>T	rs1164726138
NM_001083962.2(TCF4):c.2000A>G (p.His667Arg)	rs1555707461
NM_001083962.2(TCF4):c.305-102G>A
NM_001083962.2(TCF4):c.549+28682G>A
NM_001083962.2(TCF4):c.699G>C (p.Met233Ile)	rs1233945994
NM_001243226.3(TCF4):c.187C>T (p.Pro63Ser)
NM_001243226.3(TCF4):c.59T>G (p.Phe20Cys)	rs2148012111
NM_001243226.3(TCF4):c.74del (p.Asn25fs)	rs752700752
NM_003199.2(TCF4):c.-458A>C	rs1603624952

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