NM_001174147.2(LMX1B):c.333C>T (p.Phe111=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002152295.5
Allele description [Variation Report for NM_001174147.2(LMX1B):c.333C>T (p.Phe111=)]
NM_001174147.2(LMX1B):c.333C>T (p.Phe111=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024