List of variants in gene TCF3 reported as likely benign for B cell deficiency

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003200.5(TCF3):c.1713G>A (p.Glu571=)	rs143212973	0.00394
NM_003200.5(TCF3):c.1154G>A (p.Gly385Asp)	rs117006898	0.00282
NM_003200.5(TCF3):c.315G>A (p.Arg105=)	rs144176765	0.00160
NM_003200.5(TCF3):c.136G>A (p.Gly46Arg)	rs143529809	0.00039
NM_003200.5(TCF3):c.1564A>C (p.Lys522Gln)	rs201831565	0.00029
NM_003200.5(TCF3):c.823-13C>T	rs148835727	0.00019
NM_003200.5(TCF3):c.1948C>A (p.Pro650Thr)	rs7252811	0.00013
NM_003200.5(TCF3):c.1555A>G (p.Lys519Glu)	rs199682849	0.00011
NM_003200.5(TCF3):c.1636C>T (p.Arg546Trp)	rs747799051	0.00001
NM_003200.5(TCF3):c.1806G>A (p.Leu602=)	rs1376446279
NM_003200.5(TCF3):c.607G>A (p.Ala203Thr)	rs138005323
NM_003200.5(TCF3):c.760G>A (p.Gly254Ser)
NM_003200.5(TCF3):c.879CTC[1] (p.Ser295del)	rs550914200

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