NM_018670.4(MESP1):c.147C>T (p.Asp49=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 7, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002076753.5
Allele description [Variation Report for NM_018670.4(MESP1):c.147C>T (p.Asp49=)]
NM_018670.4(MESP1):c.147C>T (p.Asp49=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024