NM_007327.4(GRIN1):c.1633-12G>A AND Intellectual disability, autosomal dominant 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003528592.2
Allele description [Variation Report for NM_007327.4(GRIN1):c.1633-12G>A]
NM_007327.4(GRIN1):c.1633-12G>A
Condition(s)
-
hyaluronan synthase 3 isoform a [Homo sapiens]
hyaluronan synthase 3 isoform a [Homo sapiens]gi|20302153|ref|NP_005320.2|Protein
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Last Updated: Sep 29, 2024