NM_001113378.2(FANCI):c.1657C>A (p.Leu553Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003264294.2
Allele description [Variation Report for NM_001113378.2(FANCI):c.1657C>A (p.Leu553Met)]
NM_001113378.2(FANCI):c.1657C>A (p.Leu553Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
eggc.vippPP (0)
BioProject
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Last Updated: May 1, 2024