NM_000142.5(FGFR3):c.1879G>A (p.Glu627Lys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002517390.3
Allele description [Variation Report for NM_000142.5(FGFR3):c.1879G>A (p.Glu627Lys)]
NM_000142.5(FGFR3):c.1879G>A (p.Glu627Lys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Oct 20, 2024