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Gene: SLCO1B1 & Disease: HBLRR, 112 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
37346	SLCO1B1	c.521T>C	p.Val174Ala (p.V174A)	NM_006446.5 M	SNV	P	2 +	63
307954	SLCO1B1	c.1463G>C	p.Gly488Ala (p.G488A)	NM_006446.5 M	SNV	LB	1 +	9
882039	SLCO1B1	c.1007C>G	p.Pro336Arg (p.P336R)	NM_006446.5 M	SNV	B	1 +	7
30437	SLCO1B1	c.1738C>T	p.Arg580Ter (p.R580X)	NM_006446.5 M	SNV	P	1 +	5
30439	SLCO1B1	c.757C>T	p.Arg253Ter (p.R253X)	NM_006446.5 M	SNV	P	1 +	3
811089	SLCO1B1	c.664A>G	p.Ile222Val (p.I222V)	NM_006446.5 M	SNV	B	1 +	2
883909	SLCO1B1	c.452A>G	p.Asn151Ser (p.N151S)	NM_006446.5 M	SNV	B	1 +	2
307946	SLCO1B1	c.1200C>G	p.Phe400Leu (p.F400L)	NM_006446.5 M	SNV	LB	1 +	2
881968	SLCO1B1	c.170G>A	p.Arg57Gln (p.R57Q)	NM_006446.5 M	SNV	VUS	1 +	2
1034278	SLCO1B1	c.1592C>G	p.Thr531Arg (p.T531R)	NM_006446.5 M	SNV	VUS	1 +	1
880703	SLCO1B1	c.2032C>T	p.His678Tyr (p.H678Y)	NM_006446.5 M	SNV	VUS	1 +	1
1252928	SLCO1B1	c.727+33C>T	--	NM_006446.5 M	SNV	B	1 +	1
307938	SLCO1B1	c.481+1G>T	--	NM_006446.5 M	SNV	P	1 +	1
307939	SLCO1B1	c.633A>G	p.Ile211Met (p.I211M)	NM_006446.5 M	SNV	LB	1 +	1
307944	SLCO1B1	c.1086C>T	p.Tyr362= (p.Y362=)	NM_006446.5 M	SNV	B	1 +	1
307958	SLCO1B1	c.1794G>A	p.Thr598= (p.T598=)	NM_006446.5 M	SNV	LB	1 +	1
2436087	SLCO1B1	c.674C>T	p.Thr225Ile (p.T225I)	NM_006446.5 M	SNV	VUS	1 +	1
2436089	SLCO1B1	c.1213G>A	p.Val405Ile (p.V405I)	NM_006446.5 M	SNV	VUS	1 +	1
2436090	SLCO1B1	c.808A>C	p.Ile270Leu (p.I270L)	NM_006446.5 M	SNV	VUS	1 +	1
2366275	SLCO1B1	c.1474T>A	p.Ser492Thr (p.S492T)	NM_006446.5 M	SNV	VUS	1 +	1

112 Results, 20 per Page

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