NM_007192.4(SUPT16H):c.3085C>T (p.Arg1029Cys) AND Neurodevelopmental disorder with dysmorphic facies and thin corpus callosum
- Germline classification:
- Uncertain significance (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004547242.1
Allele description [Variation Report for NM_007192.4(SUPT16H):c.3085C>T (p.Arg1029Cys)]
NM_007192.4(SUPT16H):c.3085C>T (p.Arg1029Cys)
Condition(s)
Assertion and evidence details
Last Updated: May 19, 2024