NM_001371623.1(TCOF1):c.1130C>T (p.Pro377Leu) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- May 4, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001587294.4
Allele description [Variation Report for NM_001371623.1(TCOF1):c.1130C>T (p.Pro377Leu)]
NM_001371623.1(TCOF1):c.1130C>T (p.Pro377Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024