NM_007327.4(GRIN1):c.2064C>T (p.Ser688=) AND Intellectual disability, autosomal dominant 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002971713.2
Allele description [Variation Report for NM_007327.4(GRIN1):c.2064C>T (p.Ser688=)]
NM_007327.4(GRIN1):c.2064C>T (p.Ser688=)
Condition(s)
-
Same Parent, Connectivity for PubChem Compound (Select 73354857) (1)
PubChem Compound
-
Homologene neighbors for GEO Profiles (Select 125821173) (0)
GEO Profiles
-
Profile neighbors for GEO Profiles (Select 103825274) (129)
GEO Profiles
-
Related DataSets for GEO Profiles (Select 125863044) (1)
GEO DataSets
-
Hutchinson Gilford Progeria Syndrome cell line response to oncogenic challenge
Hutchinson Gilford Progeria Syndrome cell line response to oncogenic challengeAccession: GDS5426GEO DataSets
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024