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The mutations varied from person to person but were concentrated in genes known to be involved in brain development.
The frequency of these mutations varied from 0 to 8 in the mother child pairs.
The range of changes to localizations of mutations varied from one to five, the highest being for Gtm proteins.
The confidence levels of evaluated mutations varied from V2 to V4, and all tested mutations were experimentally confirmed as viable.
However, the density of mutations varied from 1/114 kb to 1/51 kb depending on the EMS dose used to generate the lines, a two-fold variation being found between 25 and 40 mM (Table 1).
In other Asian countries, the most frequent mutations varied from IVS-I-1 IVS-I-1 IVS-I-1 IVS-I-5 (G>T) in PakIndia [ 16], to −28 (A>G) in Southern China [ 13].
Similar(53)
The mutations vary from a single change in one of the nucleotide bases that constitute the gene to the deletion of the entire gene.
The frequency of these mutations varies from approximately 30% overall up to 50% in patients with a normal karyotype.
The levels of mutant SOD1 in spinal ventral horns of patients carrying SOD1 mutations vary from equal [15] to around 1% of controls [9].
Mutations vary from point mutations to null expression [136].
Moreover, it is known that the sign and the magnitude of epistasis between mutations vary from one host to another for TEV [ 29].
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