NM_173651.4(FSIP2):c.1247T>C (p.Ile416Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004124487.1
Allele description [Variation Report for NM_173651.4(FSIP2):c.1247T>C (p.Ile416Thr)]
NM_173651.4(FSIP2):c.1247T>C (p.Ile416Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024