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Letters257 J Med Genet 2001;38:257262A distinct splice form of APC is highly expressed in neurons but not commonly mutated in neuroepithelial tumors Editor APC tumor suppressor gene contains at least
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A distinct splice form is a document used to report any changes or modifications made to a specific section or portion of a gene's DNA sequence.
Researchers or scientists involved in genetic studies or gene editing are typically required to file a distinct splice form.
To fill out a distinct splice form, you need to provide details about the specific splice variant being reported, including its location, sequence, and any related functional implications. Additionally, you may need to provide information about the research methodology and supporting evidence.
The purpose of a distinct splice form is to track and document genetic variations that occur in the splicing process, which can have important implications for understanding gene function and potential genetic disorders.
A distinct splice form typically requires information about the specific splice junctions, location of the splice variant, nucleotide sequence changes, exon and intron boundaries, as well as any relevant functional annotations.
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