PMID: 20602612

Grover S, Gourie-Devi M, Baghel R, Sharma S, Bala K, Gupta M, Narayanasamy K, Varma B, Gupta M, Kaur K, Talwar P, Kaur H, Giddaluru S, Sharma A, Brahmachari SK, Indian Genome Variation Consortium, Kukreti R
Genetic profile of patients with epilepsy on first-line antiepileptic drugs and potential directions for personalized treatment.
Pharmacogenomics. 2010 Jul;11(7):927-41., [PubMed]
Sentences
No. Mutations Sentence Comment
140 ABCB1 p.Gly211Ala
X
ABCB1 p.Gly211Ala 20602612:140:78
status: NEW
view ABCB1 p.Gly211Ala details
 UGT1A1*6 is one of the most common UGT1A1 coding variants, characterized by a G211A transition corresponding to codon 71 in exon 1, which changes glycine to arginine. Login to comment