NM_002546.4(TNFRSF11B):c.256G>A (p.Val86Met) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001887520.4
Allele description [Variation Report for NM_002546.4(TNFRSF11B):c.256G>A (p.Val86Met)]
NM_002546.4(TNFRSF11B):c.256G>A (p.Val86Met)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens chemokine (C-X-C motif) ligand 2 (CXCL2), mRNA
Homo sapiens chemokine (C-X-C motif) ligand 2 (CXCL2), mRNAgi|142363029|ref|NM_002089.2|Nucleotide
-
Rattus norvegicus transducer of ErbB-2.1 (Tob1), mRNA
Rattus norvegicus transducer of ErbB-2.1 (Tob1), mRNAgi|82617613|ref|NM_133317.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024