ABCC2 p.Val1188Gln
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PMID: 22027652
[PubMed]
Elens L et al: "Functional defect caused by the 4544G>A SNP in ABCC2: potential impact for drug cellular disposition."
No.
Sentence
Comment
220
Of considerable interest for further studies, the 4544G > A SNP is in strong linkage disequilibrium in vivo with the ABCC2 rs17222723 SNP, which leads to a glutamine to valine substitution at position 1188 in ABCC2: the functional consequences of this SNP remain unexplored.
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ABCC2 p.Val1188Gln 22027652:220:156
status: NEW