NM_000142.5(FGFR3):c.1182G>A (p.Thr394=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Nov 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001594007.8
Allele description [Variation Report for NM_000142.5(FGFR3):c.1182G>A (p.Thr394=)]
NM_000142.5(FGFR3):c.1182G>A (p.Thr394=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024