NM_005928.4(MFGE8):c.339G>C (p.Met113Ile) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 5, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004304473.1
Allele description [Variation Report for NM_005928.4(MFGE8):c.339G>C (p.Met113Ile)]
NM_005928.4(MFGE8):c.339G>C (p.Met113Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 25, 2024