sequence_variant_causing_non_synonymous_codon_change_in_transcript SO_1000058
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.
Open in VFB 3D Browser →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 |