NM_000372.5(TYR):c.285C>T (p.Phe95=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 9, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003850297.1
Allele description [Variation Report for NM_000372.5(TYR):c.285C>T (p.Phe95=)]
NM_000372.5(TYR):c.285C>T (p.Phe95=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024