NM_133642.5(LARGE1):c.1584C>T (p.Asn528=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000874921.7
Allele description [Variation Report for NM_133642.5(LARGE1):c.1584C>T (p.Asn528=)]
NM_133642.5(LARGE1):c.1584C>T (p.Asn528=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024