NM_001367949.2(FAT3):c.2899C>T (p.Leu967=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 21, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001670707.2
Allele description [Variation Report for NM_001367949.2(FAT3):c.2899C>T (p.Leu967=)]
NM_001367949.2(FAT3):c.2899C>T (p.Leu967=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023