NM_005249.5(FOXG1):c.424C>G (p.Pro142Ala) AND Rett syndrome, congenital variant
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003515153.2
Allele description [Variation Report for NM_005249.5(FOXG1):c.424C>G (p.Pro142Ala)]
NM_005249.5(FOXG1):c.424C>G (p.Pro142Ala)
Condition(s)
-
MAG: hypothetical protein A3D53_01060 [Candidatus Magasanikbacteria bacterium RI...
MAG: hypothetical protein A3D53_01060 [Candidatus Magasanikbacteria bacterium RIFCSPHIGHO2_02_FULL_45_10]gi|1083682031|gb|OGH69345.1||gnl|WG A|A3D53_01060Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024