NM_015295.3(SMCHD1):c.5127G>T (p.Ser1709=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 23, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000731981.6
Allele description [Variation Report for NM_015295.3(SMCHD1):c.5127G>T (p.Ser1709=)]
NM_015295.3(SMCHD1):c.5127G>T (p.Ser1709=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024