NM_002449.5(MSX2):c.117C>T (p.Arg39=) AND Cranium bifidum occultum
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002151737.7
Allele description [Variation Report for NM_002449.5(MSX2):c.117C>T (p.Arg39=)]
NM_002449.5(MSX2):c.117C>T (p.Arg39=)
Condition(s)
- Name:
- Cranium bifidum occultum
- Synonyms:
- CRANIUM BIFIDUM, HEREDITARY; Enlarged parietal foramina; CATLIN MARKS
- Identifiers:
- MedGen: C1868598; Human Phenotype Ontology: HP:0004423
Assertion and evidence details
Last Updated: Feb 28, 2024