NM_003072.5(SMARCA4):c.1099C>T (p.Leu367=) AND Coffin-Siris syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000397430.13
Allele description [Variation Report for NM_003072.5(SMARCA4):c.1099C>T (p.Leu367=)]
NM_003072.5(SMARCA4):c.1099C>T (p.Leu367=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024