Mutation, Missense [missense mutace]

topical
212
Terms

mutace měnící smysl kodonu

Persistent link   https://www.medvik.cz/link/D020125
Definition

A mutation in which a codon is mutated to one directing the incorporation of a different amino acid. This substitution may result in an inactive or unstable product. (From A Dictionary of Genetics, King & Stansfield, 5th ed)

DUI
D020125 MeSH Browser
CUI
M0029865
Previous indexing
Amino Acid Sequence (1966-1998)
History note
1999
Public note
1999

G Phenomena and Processes
G03 Metabolism 1 197
G05.365.590 Mutation 4 997
G05.365.590.029 Allelic Imbalance 2
G05.365.590.060 Base Pair Mismatch 14
G05.365.590.175 Chromosome Aberrations 1 574
G05.365.590.195 Codon, Nonsense 52
G05.365.590.220 DNA Repeat Expansion 7
G05.365.590.265 Frameshift Mutation 47
G05.365.590.288 Gain of Function Mutation 18
G05.365.590.310 Gene Amplification 333
G05.365.590.320 Gene Duplication 65
G05.365.590.335 Genomic Instability 87
G05.365.590.350 Germ-Line Mutation 199
G05.365.590.500 INDEL Mutation 17
G05.365.590.538 Loss of Function Mutation 12
G05.365.590.575 Mutagenesis, Insertional 56
G05.365.590.594 Mutation Accumulation 3
G05.365.590.612 Mutation Rate 18
G05.365.590.650 Mutation, Missense 212
G05.365.590.675 Point Mutation 246
G05.365.590.762 Sequence Deletion 104
G05.365.590.770 Sequence Inversion 2
G05.365.590.803 Silent Mutation 2
G05.365.590.835 Suppression, Genetic 29