PMID: 17652833

Bartnicka L, Kurzawski M, Drozdzik A, Plonska-Gosciniak E, Gornik W, Drozdzik M
Effect of ABCB1 (MDR1) 3435C >T and 2677G >A,T polymorphisms and P-glycoprotein inhibitors on salivary digoxin secretion in congestive heart failure patients.
Pharmacol Rep. 2007 May-Jun;59(3):323-9., [PubMed]
Sentences
No. Mutations Sentence Comment
24 ABCC1 p.Ala893Ser
X
ABCC1 p.Ala893Ser 17652833:24:222
status: NEW
view ABCC1 p.Ala893Ser details
ABCC1 p.Ala893Thr
X
ABCC1 p.Ala893Thr 17652833:24:208
status: NEW
view ABCC1 p.Ala893Thr details
 The 3435C >T SNP is a silent mutation that does not cause amino acid substitution and is suggested to be linked, in a majority of subjects, with the mutation in exon 21, position 2677 (2677G >T,A), producing Ala893Thr and Ala893Ser, respectively [16]. Login to comment