NM_001110792.2(MECP2):c.553C>A (p.Pro185Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003128734.1
Allele description [Variation Report for NM_001110792.2(MECP2):c.553C>A (p.Pro185Thr)]
NM_001110792.2(MECP2):c.553C>A (p.Pro185Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Mar 4, 2023