NM_001110792.2(MECP2):c.1469G>A (p.Arg490Gln) AND Severe neonatal-onset encephalopathy with microcephaly
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001048888.8
Allele description [Variation Report for NM_001110792.2(MECP2):c.1469G>A (p.Arg490Gln)]
NM_001110792.2(MECP2):c.1469G>A (p.Arg490Gln)
Condition(s)
-
4930448A20Rik RIKEN cDNA 4930448A20 gene [Mus musculus]
4930448A20Rik RIKEN cDNA 4930448A20 gene [Mus musculus]Gene ID:73993Gene
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Last Updated: Aug 4, 2024