NM_015060.3(AVL9):c.761G>T (p.Ser254Ile) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004279408.1
Allele description [Variation Report for NM_015060.3(AVL9):c.761G>T (p.Ser254Ile)]
NM_015060.3(AVL9):c.761G>T (p.Ser254Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
txid523841[Organism] (9)
BioProject
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Last Updated: Jun 9, 2024