NM_007327.4(GRIN1):c.2148G>A (p.Glu716=) AND Intellectual disability, autosomal dominant 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002839301.2
Allele description [Variation Report for NM_007327.4(GRIN1):c.2148G>A (p.Glu716=)]
NM_007327.4(GRIN1):c.2148G>A (p.Glu716=)
Condition(s)
-
Homo sapiens CDC42 effector protein (Rho GTPase binding) 4 (CDC42EP4), mRNA
Homo sapiens CDC42 effector protein (Rho GTPase binding) 4 (CDC42EP4), mRNAgi|14165470|ref|NM_012121.3|Nucleotide
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Last Updated: Feb 20, 2024