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Gene: SLCO1B3-SLCO1B7 & Disease: HBLRR, 70 results

ClinVar	Gene	Nucleotide	Amino Acid	Transcript ID	Mutation type	Clinical Significance	Disease count	Publications
30488	SLCO1B3-SLCO1B7	c.1747+1G>A	--	NM_001371097.1	SNV	P	1 +	3
2436096	SLCO1B3-SLCO1B7	c.1364C>G	p.Pro455Arg (p.P455R)	NM_001371097.1	SNV	VUS	1 +	1
2436097	SLCO1B3-SLCO1B7	c.170_174del	p.Arg57fs (p.R57fs)	NM_001371097.1	Del	VUS	1 +	1
2436098	SLCO1B3-SLCO1B7	c.1147A>G	p.Ile383Val (p.I383V)	NM_001371097.1	SNV	VUS	1 +	1
2436099	SLCO1B3-SLCO1B7	c.1865+14691T>A	--	NM_001371097.1	SNV	VUS	1 +	1
2436100	SLCO1B3-SLCO1B7	c.1291G>A	p.Glu431Lys (p.E431K)	NM_001371097.1	SNV	VUS	1 +	1
2436101	SLCO1B3-SLCO1B7	c.67C>T	p.Arg23Cys (p.R23C)	NM_001371097.1	SNV	VUS	1 +	1
2436102	SLCO1B3-SLCO1B7	c.956C>G	p.Thr319Ser (p.T319S)	NM_001371097.1	SNV	VUS	1 +	1
2436105	SLCO1B3-SLCO1B7	c.1363C>G	p.Pro455Ala (p.P455A)	NM_001371097.1	SNV	VUS	1 +	1
2436104	SLCO1B3-SLCO1B7	c.1241C>A	p.Thr414Asn (p.T414N)	NM_001371097.1	SNV	VUS	1 +	1
2436107	SLCO1B3-SLCO1B7	c.1685T>C	p.Ile562Thr (p.I562T)	NM_001371097.1	SNV	VUS	1 +	1
2436108	SLCO1B3-SLCO1B7	c.1205T>C	p.Leu402Ser (p.L402S)	NM_001371097.1	SNV	VUS	1 +	1
2436109	SLCO1B3-SLCO1B7	c.1274A>G	p.Tyr425Cys (p.Y425C)	NM_001371097.1	SNV	VUS	1 +	1
2436106	SLCO1B3-SLCO1B7	c.446_448del	p.Ser149Del (p.S149del)	NM_001371097.1	Del	VUS	1 +	1
883729	SLCO1B3-SLCO1B7	c.434A>G	p.Asn145Ser (p.N145S)	NM_001371097.1	SNV	B	1 +	1
727114	SLCO1B3-SLCO1B7	c.1101C>T	p.Tyr367= (p.Y367=)	NM_001371097.1	SNV	LB	1 +	1
993882	SLCO1B3-SLCO1B7	c.1309G>A	p.Gly437Ser (p.G437S)	NM_001371097.1	SNV	VUS	1 +	1
719501	SLCO1B3-SLCO1B7	c.69C>T	p.Arg23= (p.R23=)	NM_001371097.1	SNV	B	1 +	1
736406	SLCO1B3-SLCO1B7	c.801A>G	p.Leu267= (p.L267=)	NM_001371097.1	SNV	B	1 +	1
881835	SLCO1B3-SLCO1B7	c.645A>G	p.Ile215Met (p.I215M)	NM_001371097.1	SNV	VUS	1 +	1

70 Results, 20 per Page

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