rare_amino_acid_variant    (CURRENT_SVN)

SO Accession: SO:0002008 (SOWiki)
Definition: A sequence variant whereby at least one base of a codon encoding a rare amino acid is changed, resulting in a different encoded amino acid.
Synonyms: Jannovar:rare_amino_acid_variant, rare amino acid variant, snpEff:RARE_AMINO_ACID
DB Xrefs: SO: ke

Parent: non_conservative_missense_variant (SO:0001586)

Children: selenocysteine_loss (SO:0002009)
pyrrolysine_loss (SO:0002010)
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