NM_022725.4(FANCF):c.959C>T (p.Pro320Leu) AND not specified
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Feb 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000121025.8
Allele description [Variation Report for NM_022725.4(FANCF):c.959C>T (p.Pro320Leu)]
NM_022725.4(FANCF):c.959C>T (p.Pro320Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 19, 2024
SCV000085193