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Gene: RELN & Disease: LIS2, 4734 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
521887	RELN	c.2359G>T	p.Ala787Ser (p.A787S)	NM_005045.4 M	SNV	VUS	2 +	9
521887	RELN	c.2359G>T	p.Ala787Ser (p.A787S)	NM_173054.3	SNV	VUS	2 +	9
130127	RELN	c.5284G>A	p.Val1762Ile (p.V1762I)	NM_005045.4 M	SNV	P	4 +	7
130127	RELN	c.5284G>A	p.Val1762Ile (p.V1762I)	NM_173054.3	SNV	P	4 +	7
130125	RELN	c.5108C>G	p.Pro1703Arg (p.P1703R)	NM_005045.4 M	SNV	LB	2 +	5
130125	RELN	c.5108C>G	p.Pro1703Arg (p.P1703R)	NM_173054.3	SNV	LB	2 +	5
1066513	RELN	c.2303+1G>A	--	NM_005045.4 M	SNV	LP	2 +	4
1066813	RELN	c.5615-2A>G	--	NM_005045.4 M	SNV	LP	2 +	4
2091013	RELN	c.473+1G>A	--	NM_005045.4 M	SNV	LP	2 +	4
2066650	RELN	c.8843+2T>C	--	NM_005045.4 M	SNV	LP	2 +	4
95223	RELN	c.5711C>T	p.Thr1904Met (p.T1904M)	NM_005045.4 M	SNV	LB	3 +	4
1186074	RELN	c.3912+2T>G	--	NM_005045.4 M	SNV	LP	2 +	4
130126	RELN	c.5156C>T	p.Ser1719Leu (p.S1719L)	NM_005045.4 M	SNV	LB	2 +	4
1474142	RELN	c.7180+1G>T	--	NM_005045.4 M	SNV	LP	2 +	4
1676406	RELN	c.7349+2T>C	--	NM_005045.4 M	SNV	LP	2 +	4
1066513	RELN	c.2303+1G>A	--	NM_173054.3	SNV	LP	2 +	4
1066813	RELN	c.5615-2A>G	--	NM_173054.3	SNV	LP	2 +	4
2091013	RELN	c.473+1G>A	--	NM_173054.3	SNV	LP	2 +	4
2066650	RELN	c.8843+2T>C	--	NM_173054.3	SNV	LP	2 +	4
95223	RELN	c.5711C>T	p.Thr1904Met (p.T1904M)	NM_173054.3	SNV	LB	3 +	4

4734 Results, 20 per Page

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