NM_024597.4(MAP7D3):c.1011A>G (p.Ser337=) AND not provided
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Sep 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000965530.11
Allele description [Variation Report for NM_024597.4(MAP7D3):c.1011A>G (p.Ser337=)]
NM_024597.4(MAP7D3):c.1011A>G (p.Ser337=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024