ABCG2 p.Phe507Ser

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PMID: 15475413 [PubMed] Kobayashi D et al: "Functional assessment of ABCG2 (BCRP) gene polymorphisms to protein expression in human placenta."
No. Sentence Comment
116 Another polymorphism, a C1515 deletion, which results in a frame shift (Phe506Ser, Phe507Ser, Val508Leu, and Met509stop), was extremely rare (0.5%) in our samples.
ABCG2 p.Phe507Ser 15475413:116:83
status: VERIFIED
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