NM_000372.5(TYR):c.1161T>C (p.Leu387=) AND not provided
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Jan 17, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000732306.12
Allele description [Variation Report for NM_000372.5(TYR):c.1161T>C (p.Leu387=)]
NM_000372.5(TYR):c.1161T>C (p.Leu387=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 9, 2024