NM_000551.4(VHL):c.221T>C (p.Val74Ala) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000698497.7
Allele description [Variation Report for NM_000551.4(VHL):c.221T>C (p.Val74Ala)]
NM_000551.4(VHL):c.221T>C (p.Val74Ala)
Condition(s)
-
interferon alpha-inducible protein 27, mitochondrial isoform 1 [Homo sapiens]
interferon alpha-inducible protein 27, mitochondrial isoform 1 [Homo sapiens]gi|572879007|ref|NP_001275885.1|Protein
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Last Updated: Sep 29, 2024