NM_001041.4(SI):c.417T>G (p.Phe139Leu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001997880.6
Allele description [Variation Report for NM_001041.4(SI):c.417T>G (p.Phe139Leu)]
NM_001041.4(SI):c.417T>G (p.Phe139Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024