NM_000142.5(FGFR3):c.1248C>T (p.Arg416=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003038585.3
Allele description [Variation Report for NM_000142.5(FGFR3):c.1248C>T (p.Arg416=)]
NM_000142.5(FGFR3):c.1248C>T (p.Arg416=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
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Last Updated: Sep 29, 2024