|
Criado por gina_evans0312
mais de 10 anos atrás
|
|
Activating Mutation
Deactivating mutation
Nucleotide substitution
Nucleotide substitution in Hereditary Haemachromatosis
Synonymous Mutation
Missense Mutation
Nonsense mutation
Nucleotide deletions/insertions
Splicing Mutations
Copy Number Variation
Genomic Disorders
DiGeorge Syndrome
CNV Occurence
Gene disruption
Gene fusion
Revealing positional effects