NM_000128.4(F11):c.1179G>A (p.Ala393=) AND F11-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003900388.1
Allele description [Variation Report for NM_000128.4(F11):c.1179G>A (p.Ala393=)]
NM_000128.4(F11):c.1179G>A (p.Ala393=)
Condition(s)
- Name:
- F11-related disorder
- Synonyms:
- F11-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 26, 2024