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Gene: LRP6 & Disease: STHAG7, 80 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
1255586	LRP6	c.3406C>T	p.Arg1136Trp (p.R1136W)	NM_002336.3 M	SNV	VUS	2 +	2
723536	LRP6	c.3192A>G	p.Val1064= (p.V1064=)	NM_002336.3 M	SNV	B	2 +	2
723537	LRP6	c.2382C>T	p.Asn794= (p.N794=)	NM_002336.3 M	SNV	B	2 +	2
1805121	LRP6	c.3332dup	p.Ser1111fs (p.S1111fs)	NM_002336.3 M	Dup	P	1 +	2
620374	LRP6	c.1003C>T	p.Arg335Ter (p.R335X)	NM_002336.3 M	SNV	P	1 +	2
1805121	LRP6	c.3332dup	p.Ser1111Argfs (p.S1111Argfs)	NM_001414244.1	Dup	P	1 +	2
	LRP6	c.3332dup	p.Ser1111Argfs (p.S1111Argfs)	NM_001414245.1	Dup	P	1 +	2
	LRP6	c.3332dup	p.Ser1111Argfs (p.S1111Argfs)	NM_001414246.1	Dup	P	1 +	2
	LRP6	c.3134dup	p.Ser1045Argfs (p.S1045Argfs)	NM_001414247.1	Dup	P	1 +	2
	LRP6	c.3332dup	p.Ser1111Argfs (p.S1111Argfs)	NM_001414248.1	Dup	P	1 +	2
	LRP6	c.3332dup	p.Ser1111Argfs (p.S1111Argfs)	NM_001414249.1	Dup	P	1 +	2
	LRP6	c.3332dup	p.Ser1111Argfs (p.S1111Argfs)	NM_001414250.1	Dup	P	1 +	2
	LRP6	c.3332dup	p.Ser1111Argfs (p.S1111Argfs)	NM_001414251.1	Dup	P	1 +	2
	LRP6	c.2879dup	p.Ser960Argfs (p.S960Argfs)	NM_001414252.1	Dup	P	1 +	2
	LRP6	c.2879dup	p.Ser960Argfs (p.S960Argfs)	NM_001414253.1	Dup	P	1 +	2
	LRP6	c.2879dup	p.Ser960Argfs (p.S960Argfs)	NM_001414254.1	Dup	P	1 +	2
	LRP6	c.2825dup	p.Ser942Argfs (p.S942Argfs)	NM_001414255.1	Dup	P	1 +	2
1342139	LRP6	c.3399del	p.Ala1134fs (p.A1134fs)	NM_002336.3 M	Del	P	1 +	1
1199176	LRP6	c.845-1G>A	--	NM_002336.3 M	SNV	P	1 +	1
1033503	LRP6	c.3394_3395del	p.Ser1132fs (p.S1132fs)	NM_002336.3 M	MS	P	1 +	1

80 Results, 20 per Page

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