NM_001291303.3(FAT4):c.1176G>C (p.Gly392=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003827155.2
Allele description [Variation Report for NM_001291303.3(FAT4):c.1176G>C (p.Gly392=)]
NM_001291303.3(FAT4):c.1176G>C (p.Gly392=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024