NM_000178.4(GSS):c.1332C>T (p.His444=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003738419.1
Allele description [Variation Report for NM_000178.4(GSS):c.1332C>T (p.His444=)]
NM_000178.4(GSS):c.1332C>T (p.His444=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024