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Gene: TCF3 & Disease: AGM8B, 52 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
1607823	TCF3	c.823-13C>T	--	NM_003200.5 M	SNV	LB	2 +	2
717103	TCF3	c.1713G>A	p.Glu571= (p.E571=)	NM_003200.5 M	SNV	LB	2 +	2
709097	TCF3	c.1948C>A	p.Pro650Thr (p.P650T)	NM_003200.5 M	SNV	LB	2 +	2
1432193	TCF3	c.1430G>A	p.Arg477Gln (p.R477Q)	NM_003200.5 M	SNV	VUS	2 +	2
719522	TCF3	c.315G>A	p.Arg105= (p.R105=)	NM_003200.5 M	SNV	LB	2 +	2
735931	TCF3	c.1564A>C	p.Lys522Gln (p.K522Q)	NM_003200.5 M	SNV	LB	2 +	2
730318	TCF3	c.307G>A	p.Gly103Ser (p.G103S)	NM_003200.5 M	SNV	LB	2 +	2
1051931	TCF3	c.1327-3C>A	--	NM_003200.5 M	SNV	VUS	2 +	2
626027	TCF3	c.229G>A	p.Glu77Lys (p.E77K)	NM_003200.5 M	SNV	VUS	2 +	2
1607823	TCF3	c.823-13C>T	--	NM_001136139.4 MP	SNV	LB	2 +	2
717103	TCF3	c.1586+292G>A	--	NM_001136139.4 MP	SNV	LB	2 +	2
709097	TCF3	c.1939C>A	p.Pro647Thr (p.P647T)	NM_001136139.4 MP	SNV	LB	2 +	2
1432193	TCF3	c.1430G>A	p.Arg477Gln (p.R477Q)	NM_001136139.4 MP	SNV	VUS	2 +	2
719522	TCF3	c.315G>A	p.Arg105= (p.R105=)	NM_001136139.4 MP	SNV	LB	2 +	2
735931	TCF3	c.1564A>C	p.Lys522Gln (p.K522Q)	NM_001136139.4 MP	SNV	LB	2 +	2
730318	TCF3	c.307G>A	p.Gly103Ser (p.G103S)	NM_001136139.4 MP	SNV	LB	2 +	2
1051931	TCF3	c.1327-3C>A	--	NM_001136139.4 MP	SNV	VUS	2 +	2
626027	TCF3	c.229G>A	p.Glu77Lys (p.E77K)	NM_001136139.4 MP	SNV	VUS	2 +	2
1607823	TCF3	c.823-13C>T	--	NM_001351778.2	SNV	LB	2 +	2
1607823	TCF3	c.823-13C>T	--	NM_001351779.2	SNV	LB	2 +	2

52 Results, 20 per Page

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