corsepiu - c++/6465: Segfault on conflicting types
M1180I+x9xJ1PjubKRBycMokYoORaAaxTWJgZaaYTM65jxGF93vj4nTqrScjp4vNJO84QrZheltL
BTK mutation database: K11
INSULIN RECEPTOR; IRK; ; M1180I; g3678a. Accession K11 Date 2-Mar-1998 (Rel. 1, Created) Date 2-Mar-1998 (Rel. 1, Last updated, Version 1)
Kinase Mutation Database maintained by Kaj Stenberg programmed by
IRK; ; M1180I; g3678a Accession K11 Date 2-Mar-1998 (Rel. 1, Created) Date 2-Mar-1998 (Rel. 1, Last updated, Version 1) RefNumber 1 RefAuthors Cama A,
Receptors for insulin & insulin-like molecules
M1180I. Original amino acid/Mutated amino acid, M /I. Type of mutation, Naturally occurring substitution. Associated disorder, Insulin-resistant diabetes
Receptors for insulin & insulin-like molecules
M1180I (Reference sequence P06213 ). Type of mutation, Naturally occurring. Codon change, ATG to ATC or ATT or ATA. Changed nucleotide number, 3678
SNP PhenoClass Environ SecStruct AreaBuried FracPolar ScopLink
INSR_HUMAN:W1220L Disease B3 H 0.997 0.448 d1ir3a_ 0.03 11 INSR_HUMAN:G393R Disease E C 0.159 0.698 d1igra2 0.02 12 INSR_HUMAN:M1180I Disease B3 C 0.600 m1180i: m1180i