Amino acid replacement: W337term.
Mutation is in exon 9, an exon common to all alternative splice isoforms.
G9798197A
G?A
W337term | nAChRalpha6-PA; W337term | nAChRalpha6-PB; W337term | nAChRalpha6-PC; W352term | nAChRalpha6-PD; W366term | nAChRalpha6-PE; W337term | nAChRalpha6-PG; W337term | nAChRalpha6-PH
W337term
G to A nucleotide change at the second or third position of the Trp codon leads to a nonsense mutation (exact site of mutation unspecified).