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insertion mutation
frameshift mutation - can change the amino acid sequence, affecting protein structure. this mutation changes the amino acid that would have been coded for the original base triplet (eg. ACC → ACG)
deletion mutation
base is randomly deleted from the DNA sequence
frameshift mutation - can change structure of protein
silent mutations
mutation does not alter amino acid sequence of polypeptide
missense mutations
alters a single amino acid in the polypeptide chain (eg. sickle cell anaemia)
nonsense mutations
creates a premature stop codon - polypeptide chain will be incomplete, affecting protein structure
beneficial mutations
altered characteristic which causes beneficial affects eg. melanin production providing protection from UV radiation
harmful mutations
altered characteristic which causes harmful effects for the organisms (eg. cystic fibrosis, CFTR protein and deletion mutations)
neutral mutations
offers no selective advantage/disadvantage (eg - TAS2R38 taster ability. increased perception of bitterness)