sequence_variant_causing_non_synonymous_codon_change_in_transcript [SO_1000058]

A DNA point mutation that causes a substitution of an amino acid by an other.

sequence_variant_causing_non_synonymous_codon_change_in_transcript

ID: SO_1000058

Deprecated

A DNA point mutation that causes a substitution of an amino acid by an other.

OBSOLETE: This term was deleted as it conflated more than one term. The alteration is separate from the effect.

Alternative Names

Synonym	Scope	Reference
non-synonymous codon change in transcript	exact synonym
sequence variant causing non synonymous codon change in transcript	exact synonym
mutation causing non synonymous codon change in transcript	related synonym

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