NM_001305581.2(LRMDA):c.444C>T (p.Ala148=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002627139.3
Allele description [Variation Report for NM_001305581.2(LRMDA):c.444C>T (p.Ala148=)]
NM_001305581.2(LRMDA):c.444C>T (p.Ala148=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024