NM_005249.5(FOXG1):c.354G>C (p.Gly118=) AND Rett syndrome, congenital variant
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003847957.1
Allele description [Variation Report for NM_005249.5(FOXG1):c.354G>C (p.Gly118=)]
NM_005249.5(FOXG1):c.354G>C (p.Gly118=)
Condition(s)
-
"433302-49-9"[CompleteSynonym] (1)
PubChem Compound
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See more...Assertion and evidence details
Last Updated: Mar 5, 2024