NM_014976.2(PDCD11):c.839C>T (p.Pro280Leu) 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:
- RCV004273398.1
Allele description [Variation Report for NM_014976.2(PDCD11):c.839C>T (p.Pro280Leu)]
NM_014976.2(PDCD11):c.839C>T (p.Pro280Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
888 eggc.vipvnB (0)
BioProject
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Last Updated: Jun 2, 2024