NM_000142.5(FGFR3):c.726G>A (p.Thr242=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003556885.2
Allele description [Variation Report for NM_000142.5(FGFR3):c.726G>A (p.Thr242=)]
NM_000142.5(FGFR3):c.726G>A (p.Thr242=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Tssr74968 AND (alive[prop]) (0)
Gene
-
Databases, Nucleic Acid
Databases, Nucleic AcidDatabases containing information about NUCLEIC ACIDS such as BASE SEQUENCE; SNPS; NUCLEIC ACID CONFORMATION; and other properties. Information about the DNA fragments kept in ...<br/>Year introduced: 2002MeSH
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Last Updated: Sep 29, 2024