NM_001113378.2(FANCI):c.2997C>T (p.Ser999=) AND not provided
- Germline classification:
- Likely benign (4 submissions)
- Last evaluated:
- Apr 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001569204.21
Allele description [Variation Report for NM_001113378.2(FANCI):c.2997C>T (p.Ser999=)]
NM_001113378.2(FANCI):c.2997C>T (p.Ser999=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 19, 2024