NM_007327.4(GRIN1):c.1751+17G>C AND Intellectual disability, autosomal dominant 8
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003843229.1
Allele description [Variation Report for NM_007327.4(GRIN1):c.1751+17G>C]
NM_007327.4(GRIN1):c.1751+17G>C
Condition(s)
-
Chromosome neighbors for GEO Profiles (Select 83391182) (18)
GEO Profiles
-
Conserved Domain Links for Gene (Select 55074) (2)
Conserved Domains
-
Homo sapiens isolate:CHM13
Homo sapiens isolate:CHM13Homo sapiens isolate:CHM13 RefSeq Genome sequencing and assemblyBioProject
-
BioProject Links for Protein (Select 2462544231) (1)
BioProject
-
Component Of for Nucleotide (Select 2328448627) (0)
Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Mar 5, 2024