NM_001370466.1(NOD2):c.379G>A (p.Asp127Asn) AND NOD2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003969902.1
Allele description [Variation Report for NM_001370466.1(NOD2):c.379G>A (p.Asp127Asn)]
NM_001370466.1(NOD2):c.379G>A (p.Asp127Asn)
Condition(s)
- Name:
- NOD2-related disorder
- Synonyms:
- NOD2-related condition
- Identifiers:
-
Homo sapiens isolate:CHM13
Homo sapiens isolate:CHM13Homo sapiens isolate:CHM13 RefSeq Genome sequencing and assemblyBioProject
-
BioProject Links for Protein (Select 2462520557) (1)
BioProject
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See more...Assertion and evidence details
Last Updated: May 19, 2024