NM_005912.3(MC4R):c.935C>G (p.Thr312Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002469815.1
Allele description [Variation Report for NM_005912.3(MC4R):c.935C>G (p.Thr312Ser)]
NM_005912.3(MC4R):c.935C>G (p.Thr312Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Dec 24, 2022