NM_002397.5(MEF2C):c.258+7G>C AND Intellectual disability, autosomal dominant 20
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 27, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001405868.13
Allele description [Variation Report for NM_002397.5(MEF2C):c.258+7G>C]
NM_002397.5(MEF2C):c.258+7G>C
Condition(s)
-
calmegin isoform X2 [Apteryx rowi]
calmegin isoform X2 [Apteryx rowi]gi|1444507607|ref|XP_025930198.1|Protein
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Last Updated: Oct 26, 2024