NM_001048166.1(STIL):c.3581C>T (p.Pro1194Leu) AND Microcephaly 7, primary, autosomal recessive
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001096323.6
Allele description [Variation Report for NM_001048166.1(STIL):c.3581C>T (p.Pro1194Leu)]
NM_001048166.1(STIL):c.3581C>T (p.Pro1194Leu)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024