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Gene: TBX22 & Disease: CPX, 168 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
11331	TBX22	c.633+1G>A	--	NM_001109878.2 M	SNV	P	1 +	3
	TBX22	c.273+1G>A	--	NM_001109879.2	SNV	P	1 +	3
	TBX22	c.633+1G>A	--	NM_016954.2	SNV	P	1 +	3
	TBX22	c.273+1G>A	--	NM_001303475.1	SNV	P	1 +	3
11329	TBX22	c.779C>T	p.Thr260Met (p.T260M)	NM_001109878.2 M	SNV	P	1 +	2
50315	TBX22	c.459-5T>A	--	NM_001109878.2 M	SNV	P	2 +	2
11329	TBX22	c.419C>T	p.Thr140Met (p.T140M)	NM_001109879.2	SNV	P	1 +	2
	TBX22	c.419C>T	p.Thr140Met (p.T140M)	NM_001303475.1	SNV	P	1 +	2
	TBX22	c.779C>T	p.Thr260Met (p.T260M)	NM_016954.2	SNV	P	1 +	2
50315	TBX22	c.99-5T>A	--	NM_001109879.2	SNV	P	2 +	2
	TBX22	c.459-5T>A	--	NM_016954.2	SNV	P	2 +	2
	TBX22	c.99-5T>A	--	NM_001303475.1	SNV	P	2 +	2
368664	TBX22	c.72C>T	p.Leu24= (p.L24=)	NM_001109878.2 M	SNV	B	1 +	1
368669	TBX22	c.949+12T>G	--	NM_001109878.2 M	SNV	LB	2 +	1
11328	TBX22	c.863+1G>C	--	NM_001109878.2 M	SNV	P	1 +	1
11330	TBX22	c.352G>T	p.Gly118Cys (p.G118C)	NM_001109878.2 M	SNV	P	1 +	1
11332	TBX22	c.667del	p.Arg223fs (p.R223fs)	NM_001109878.2 M	Del	P	1 +	1
11333	TBX22	c.166G>T	p.Glu56Ter (p.E56X)	NM_001109878.2 M	SNV	P	1 +	1
11334	TBX22	c.641T>C	p.Leu214Pro (p.L214P)	NM_001109878.2 M	SNV	P	1 +	1
11335	TBX22	c.584_586dup	p.Ser195_Phe196insCys	NM_001109878.2 M	Dup	P	1 +	1

168 Results, 20 per Page

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