NM_175736.5(FMNL3):c.1211A>G (p.His404Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 12, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004112351.1
Allele description [Variation Report for NM_175736.5(FMNL3):c.1211A>G (p.His404Arg)]
NM_175736.5(FMNL3):c.1211A>G (p.His404Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Nov 10, 2024