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Gene: BDNF & Disease: CCHS, 17 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
17696	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_001709.5 M	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_001143805.1	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_001143806.1	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_001143807.2	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_001143808.2	SNV	LB	3 +	1
	BDNF	c.92C>T	p.Thr31Ile (p.T31I)	NM_001143809.2	SNV	LB	3 +	1
	BDNF	c.251C>T	p.Thr84Ile (p.T84I)	NM_001143810.2	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_001143811.2	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_001143812.2	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_001143813.2	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_001143814.2	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_001143816.2	SNV	LB	3 +	1
	BDNF	c.29C>T	p.Thr10Ile (p.T10I)	NM_170731.5	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_170732.4	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_170733.4	SNV	LB	3 +	1
	BDNF	c.50C>T	p.Thr17Ile (p.T17I)	NM_170734.4	SNV	LB	3 +	1
	BDNF	c.5C>T	p.Thr2Ile (p.T2I)	NM_170735.6	SNV	LB	3 +	1

17 Results, 20 per Page

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