List of variants in gene TCF3 reported as uncertain significance for Agammaglobulinemia 8, autosomal dominant

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_003200.5(TCF3):c.307G>A (p.Gly103Ser)	rs201841190	0.00037
NM_003200.5(TCF3):c.473G>A (p.Arg158Gln)	rs554419240	0.00012
NM_003200.5(TCF3):c.229G>A (p.Glu77Lys)	rs138963927	0.00011
NM_003200.5(TCF3):c.23C>T (p.Ala8Val)	rs376780559	0.00008
NM_003200.5(TCF3):c.1049C>T (p.Ser350Leu)	rs963433488	0.00002
NM_003200.5(TCF3):c.107G>A (p.Arg36Gln)	rs1011180356	0.00001
NM_003200.5(TCF3):c.1589C>G (p.Pro530Arg)	rs745797783	0.00001
NM_001136139.4(TCF3):c.1755G>A (p.Lys585=)	rs1568312916
NM_003200.5(TCF3):c.1121C>A (p.Ala374Asp)	rs753137385
NM_003200.5(TCF3):c.1543GAG[2] (p.Glu517del)
NM_003200.5(TCF3):c.1670G>A (p.Arg557Gln)	rs2145853075
NM_003200.5(TCF3):c.955+204G>A	rs372121697

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