NM_144997.7(FLCN):c.1063G>A (p.Val355Ile) AND Birt-Hogg-Dube syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003500143.3
Allele description [Variation Report for NM_144997.7(FLCN):c.1063G>A (p.Val355Ile)]
NM_144997.7(FLCN):c.1063G>A (p.Val355Ile)
Condition(s)
-
Homo sapiens fibroblast growth factor 1 (FGF1), transcript variant 14, mRNA
Homo sapiens fibroblast growth factor 1 (FGF1), transcript variant 14, mRNAgi|1675158168|ref|NM_001257212.2|Nucleotide
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Last Updated: Sep 29, 2024