NM_000204.5(CFI):c.1291G>T (p.Ala431Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001874075.5
Allele description [Variation Report for NM_000204.5(CFI):c.1291G>T (p.Ala431Ser)]
NM_000204.5(CFI):c.1291G>T (p.Ala431Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 5, 2024