NM_020911.2(PLXNA4):c.83G>A (p.Arg28Gln) AND PLXNA4-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003962267.2
Allele description [Variation Report for NM_020911.2(PLXNA4):c.83G>A (p.Arg28Gln)]
NM_020911.2(PLXNA4):c.83G>A (p.Arg28Gln)
Condition(s)
- Name:
- PLXNA4-related disorder
- Synonyms:
- PLXNA4-related condition
- Identifiers:
-
Homo sapiens clathrin heavy chain linker domain containing 1 (CLHC1), RefSeqGene...
Homo sapiens clathrin heavy chain linker domain containing 1 (CLHC1), RefSeqGene on chromosome 2; nuclear gene for mitochondrial productgi|433660860|ref|NG_033063.1|Nucleotide
-
Pathogen: clinical or host-associated sample from Klebsiella sp. 10
Pathogen: clinical or host-associated sample from Klebsiella sp. 10biosample
-
Pathogen: clinical or host-associated sample from Klebsiella pneumoniae
Pathogen: clinical or host-associated sample from Klebsiella pneumoniaebiosample
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Last Updated: Oct 13, 2024