NM_018670.4(MESP1):c.182T>G (p.Leu61Arg) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002187101.5
Allele description [Variation Report for NM_018670.4(MESP1):c.182T>G (p.Leu61Arg)]
NM_018670.4(MESP1):c.182T>G (p.Leu61Arg)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 16, 2024