NM_001190274.2(FBXO11):c.93G>T (p.Pro31=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003109155.11
Allele description [Variation Report for NM_001190274.2(FBXO11):c.93G>T (p.Pro31=)]
NM_001190274.2(FBXO11):c.93G>T (p.Pro31=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jul 7, 2024