NM_017565.4(FAM20A):c.1206C>T (p.Phe402=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 15, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000888025.16
Allele description [Variation Report for NM_017565.4(FAM20A):c.1206C>T (p.Phe402=)]
NM_017565.4(FAM20A):c.1206C>T (p.Phe402=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024