ABCG2 p.Arg236*
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PMID: 23166586
[PubMed]
Kasza I et al: "Expression levels of the ABCG2 multidrug transporter in human erythrocytes correspond to pharmacologically relevant genetic variations."
No.
Sentence
Comment
107
A nonsense mutation, causing an arginine to stop codon change at codon 236 in exon 7 (c.706C.T, p.R236X, rs140207606 described previously [39,40]) was found in heterozygous form in proband 1.
X
ABCG2 p.Arg236* 23166586:107:98
status: NEW