NM_001048166.1(STIL):c.1455G>C (p.Leu485Phe) AND Microcephaly 7, primary, autosomal recessive
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000986319.10
Allele description [Variation Report for NM_001048166.1(STIL):c.1455G>C (p.Leu485Phe)]
NM_001048166.1(STIL):c.1455G>C (p.Leu485Phe)
Condition(s)
Assertion and evidence details
Last Updated: Oct 20, 2024