NM_001110792.2(MECP2):c.289C>T (p.Arg97Cys) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 20, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000487257.2
Allele description [Variation Report for NM_001110792.2(MECP2):c.289C>T (p.Arg97Cys)]
NM_001110792.2(MECP2):c.289C>T (p.Arg97Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens FRAS1 related extracellular matrix 1 (FREM1), RefSeqGene on chromos...
Homo sapiens FRAS1 related extracellular matrix 1 (FREM1), RefSeqGene on chromosome 9gi|295317327|ref|NG_017005.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024