NM_020223.4(FAM20C):c.171G>C (p.Ala57=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 7, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002157215.5
Allele description [Variation Report for NM_020223.4(FAM20C):c.171G>C (p.Ala57=)]
NM_020223.4(FAM20C):c.171G>C (p.Ala57=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024