NM_001172509.2(SATB2):c.2109C>T (p.Ser703=) AND Chromosome 2q32-q33 deletion syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000701478.9
Allele description [Variation Report for NM_001172509.2(SATB2):c.2109C>T (p.Ser703=)]
NM_001172509.2(SATB2):c.2109C>T (p.Ser703=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024