NM_001164508.2(NEB):c.1981C>T (p.Leu661=) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jun 12, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000712388.13
Allele description [Variation Report for NM_001164508.2(NEB):c.1981C>T (p.Leu661=)]
NM_001164508.2(NEB):c.1981C>T (p.Leu661=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 20, 2024