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Gene: IFNG & Disease: AA, 20 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
14722	IFNG	c.115-483AC[12]	--	NM_000619.3 M	MS	VUS	2 +	2
632201	IFNG	c.431C>A	p.Ser144Ter (p.S144X)	NM_000619.3 M	SNV	VUS	1 +	0
881295	IFNG	c.*465A>T	--	NM_000619.3 M	SNV	LB	1 +	0
310319	IFNG	c.*539A>G	--	NM_000619.3 M	SNV	B	1 +	0
310320	IFNG	c.*500C>T	--	NM_000619.3 M	SNV	LB	1 +	0
310321	IFNG	c.*180C>T	--	NM_000619.3 M	SNV	B	1 +	0
310322	IFNG	c.*107A>G	--	NM_000619.3 M	SNV	VUS	1 +	0
310323	IFNG	c.*9C>T	--	NM_000619.3 M	SNV	VUS	1 +	0
310324	IFNG	c.114+11C>T	--	NM_000619.3 M	SNV	VUS	1 +	0
310325	IFNG	c.-2C>A	--	NM_000619.3 M	SNV	VUS	1 +	0
310326	IFNG	c.-5A>G	--	NM_000619.3 M	SNV	B	1 +	0
310327	IFNG	c.-9T>C	--	NM_000619.3 M	SNV	VUS	1 +	0
310328	IFNG	c.-34T>G	--	NM_000619.3 M	SNV	VUS	1 +	0
882897	IFNG	c.183+15C>G	--	NM_000619.3 M	SNV	VUS	1 +	0
881746	IFNG	c.*231T>C	--	NM_000619.3 M	SNV	VUS	1 +	0
881747	IFNG	c.*187T>G	--	NM_000619.3 M	SNV	VUS	1 +	0
881748	IFNG	c.*22T>A	--	NM_000619.3 M	SNV	VUS	1 +	0
881749	IFNG	c.431C>T	p.Ser144Leu (p.S144L)	NM_000619.3 M	SNV	VUS	1 +	0
881750	IFNG	c.285C>T	p.Thr95= (p.T95=)	NM_000619.3 M	SNV	VUS	1 +	0
111222	IFNG	c.*93TCAA[1]	--	NM_000619.3 M	MS	VUS	1 +	0

共20个结果, 每页展示20条

Comparison