NM_001134651.2(EIF4E3):c.13C>T (p.Pro5Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004167764.1
Allele description [Variation Report for NM_001134651.2(EIF4E3):c.13C>T (p.Pro5Ser)]
NM_001134651.2(EIF4E3):c.13C>T (p.Pro5Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Conserved Domain Links for Gene (Select 268281) (6)
Conserved Domains
-
Structure Links for Conserved Domains (Select 440843) (7)
Structure
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Last Updated: Jun 2, 2024