NM_144573.4(NEXN):c.1437T>G (p.Leu479=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002130968.5
Allele description [Variation Report for NM_144573.4(NEXN):c.1437T>G (p.Leu479=)]
NM_144573.4(NEXN):c.1437T>G (p.Leu479=)
Condition(s)
-
Homo sapiens
Homo sapiensRefSeq annotation of the human reference genome assemblyBioProject
-
BioProject Links for Nucleotide (Select 2217269308) (1)
BioProject
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Last Updated: Feb 28, 2024