NM_181342.3(FKBP7):c.416T>C (p.Ile139Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 3, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004116312.1
Allele description [Variation Report for NM_181342.3(FKBP7):c.416T>C (p.Ile139Thr)]
NM_181342.3(FKBP7):c.416T>C (p.Ile139Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 26, 2024