NM_032228.6(FAR1):c.555T>C (p.Asp185=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000891987.8
Allele description [Variation Report for NM_032228.6(FAR1):c.555T>C (p.Asp185=)]
NM_032228.6(FAR1):c.555T>C (p.Asp185=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024