NM_001491.3(GCNT2):c.254C>G (p.Pro85Arg) AND GCNT2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003902375.1
Allele description [Variation Report for NM_001491.3(GCNT2):c.254C>G (p.Pro85Arg)]
NM_001491.3(GCNT2):c.254C>G (p.Pro85Arg)
Condition(s)
- Name:
- GCNT2-related disorder
- Synonyms:
- GCNT2-related condition
- Identifiers:
-
Tagln2 transgelin 2 [Mus musculus]
Tagln2 transgelin 2 [Mus musculus]Gene ID:21346Gene
-
Nucleotide Links for Protein (Select 1822009808) (2)
Nucleotide
-
Metagenome-assembled genome: BRZ_MH__bin34
Metagenome-assembled genome: BRZ_MH__bin34biosample
-
Chromosome neighbors for GEO Profiles (Select 122691726) (20)
GEO Profiles
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See more...Assertion and evidence details
Last Updated: May 12, 2024