NM_207122.2(EXT2):c.519G>C (p.Ala173=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003391069.8
Allele description [Variation Report for NM_207122.2(EXT2):c.519G>C (p.Ala173=)]
NM_207122.2(EXT2):c.519G>C (p.Ala173=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024