NM_001277313.2(FMN1):c.2446T>C (p.Cys816Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 24, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004318220.1
Allele description [Variation Report for NM_001277313.2(FMN1):c.2446T>C (p.Cys816Arg)]
NM_001277313.2(FMN1):c.2446T>C (p.Cys816Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
1882-7616[ISSN] (1)
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Last Updated: Jun 2, 2024