NM_015295.3(SMCHD1):c.5527G>A (p.Ala1843Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 10, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000284561.4
Allele description [Variation Report for NM_015295.3(SMCHD1):c.5527G>A (p.Ala1843Thr)]
NM_015295.3(SMCHD1):c.5527G>A (p.Ala1843Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 1, 2023