Loading ...
Deletion or insertion of three or a multiple of three base pairs within coding sequencesdoes ... causeframeshift mutation
Deletion of just one nucleotide in a protein - coding part of a genewill causea " frameshift mutation
insertion or deletion mutations , nonsense mutations , and splice - site mutations(passive) caused byframeshift mutations
Deletion or insertion of three or a multiple of three base pairs inside coding sequencesdoes ... causeframeshift mutation
from and insertion or deletion of nucleotide pairs in a gene(passive) is causeda frameshift mutation
the insertion or deletion of a single nucleotide ( DNA basecauseda frameshift mutation
Insertion , deletion and duplication mutationscauseFRAMESHIFT MUTATIONS
when there are insertions , deletions and duplication of the DNA bases in a gene(passive) are also causedFrameshift mutations
by any insertion or deletion of a base pair(passive) caused byFrameshift mutations
the NHEJ pathway that results in the insertion or deletion of a random base at the site of repaircausesa frameshift mutation
by the deletion or insertion of a single base(passive) caused bya frameshift mutation
The insertion or deletion of a single basecausesa frameshift mutation
Insertions and deletion of single nucleotidescan causeframeshift mutations
a base pair ... an insertion or a deletioncausesa frameshift mutation
by nucleotide insertion or deletion(passive) caused byframeshift mutations
Mutations ) insertion Results in the addition of extra DNA Insertionscan causeframeshift mutations
that cause insertion or deletion of base pairsresultingin frameshift mutation
Insertion and deletion mutationscan potentially causeframeshift mutation
by a single adenine deletion in exon 5 that results in a premature stop codon(passive) caused bya frameshift mutation
a novel deleterious homozygous four - nucleotide deletioncausingframeshift mutation
by small deletion or insertion(passive) caused byframeshift mutations
by exon 9 deletions or insertions(passive) caused byframeshift mutations
by a deletion of a base , or an insertion of a base(passive) can be causedA frameshift mutation
deletion or insertion and aberrant splicing(passive) caused byframeshift mutations
insertions or deletions of base pairscauseframeshift mutations
by one base deletion(passive) caused bya frameshift mutation
by base pair deletions(passive) caused byframeshift mutations
a single - base deletion(passive) caused bya frameshift mutation
an insertion or deletion of a nucleotide causing the reading frame to shift & the protein(passive) are caused byFrameshift mutations
by deletion or addition of nucleotide / s leading to change in the reading of the sequence(passive) are caused byFrameshift mutations
by deletion or addition of nucleotide(passive) are caused byFrameshift mutations
insertions or deletions of nucleotides(passive) are caused byFrameshift mutations
by a single base insertion on chromosome 10(passive) caused bya frameshift mutation
DELETION ... NONsense mutationresultsin FRAMESHIFT mutation
Single nucleotide INSERTION / DELETIONcausesFRAMESHIFT mutation
the insertion or deletion of a single nucleotidecauseda frameshift mutation
the insertion or deletion of a single nucleotidecauseda frameshift mutation Frameshift mutation
the addition or deletion of nucleotides(passive) are caused byFrameshift mutations
either by the addition of a nucleotide or by a deletion(passive) are causedFrameshift mutations
the deletion of one or more nucleotides(passive) can be caused byThe frameshift mutation
prematurecausingpremature
premature stop codon and production of truncated proteincausespremature stop codon and production of truncated protein
a premature stop codon and protein truncation ( 29causinga premature stop codon and protein truncation ( 29
in a truncated form of the protein encoded by the essential generesultingin a truncated form of the protein encoded by the essential gene
the leucine ( Leu ) at amino acid position 192 to become a termination codon , leading to termination of protein sequence codingcausesthe leucine ( Leu ) at amino acid position 192 to become a termination codon , leading to termination of protein sequence coding
in a premature stop codon that in turn leads to the production of a shorter proteincan resultin a premature stop codon that in turn leads to the production of a shorter protein
to premature chain termination and the expression of a receptor lacking the kinase domainleadingto premature chain termination and the expression of a receptor lacking the kinase domain
to premature termination of the protein transcriptleadsto premature termination of the protein transcript
in a premature truncation of the proteinresultin a premature truncation of the protein
to a premature stop codon after a sequence of aberrant amino acidsleadingto a premature stop codon after a sequence of aberrant amino acids
to premature truncation of protein by a stop codon ( arrowleadsto premature truncation of protein by a stop codon ( arrow
to premature truncation of proteinleadsto premature truncation of protein
a premature stop codon in the glycophorin C genecausinga premature stop codon in the glycophorin C gene
to premature stop codons , which prevent the formation of LIFR proteinleadingto premature stop codons , which prevent the formation of LIFR protein
to loss of function of the protein in developmental disorder sotos syndromeleadsto loss of function of the protein in developmental disorder sotos syndrome
in reduced activity of the protein encoded by the genemay resultin reduced activity of the protein encoded by the gene
to formation of a truncated gene productleadingto formation of a truncated gene product
in a premature stop codon in exon 4resultingin a premature stop codon in exon 4
a shift in reading frame leading to a complete change of the amino acid sequence downstream of the mutation ( i.e. , the frameshift sitecausea shift in reading frame leading to a complete change of the amino acid sequence downstream of the mutation ( i.e. , the frameshift site
in premature termination of the generesultingin premature termination of the gene
an in - exon stop codon 6 amino acids downstream of the end of the deletioncausingan in - exon stop codon 6 amino acids downstream of the end of the deletion
to a premature stop codon and premature chain terminationledto a premature stop codon and premature chain termination
to truncation of the resulting proteinleadingto truncation of the resulting protein
to premature termination of translationleadingto premature termination of translation
to premature stop codons , null mutations , and missense mutationsleadingto premature stop codons , null mutations , and missense mutations
premature stop codons , null mutations , and missense mutationsleadingpremature stop codons , null mutations , and missense mutations
in a premature stop codon in exonresultedin a premature stop codon in exon
in a truncated proteinresultingin a truncated protein
in a premature stop codon in exon 10resultingin a premature stop codon in exon 10
to truncated protein productsleadingto truncated protein products
to truncated protein productsleadto truncated protein products
in a premature stop codon and a missense mutation inresultingin a premature stop codon and a missense mutation in
to truncated proteins with impaired or no functionleadingto truncated proteins with impaired or no function
to truncated proteins with impaired functionleadingto truncated proteins with impaired function
to premature STOP codonsleadingto premature STOP codons
premature stop codonscausingpremature stop codons
in premature stop codonsresultin premature stop codons
to premature stop codonsleadto premature stop codons
premature stop codonsleadpremature stop codons
in premature stop codonsresultingin premature stop codons