NM_145728.3(SYNM):c.408G>A (p.Arg136=) AND SYNM-related disorder
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Oct 28, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003907190.1
Allele description [Variation Report for NM_145728.3(SYNM):c.408G>A (p.Arg136=)]
NM_145728.3(SYNM):c.408G>A (p.Arg136=)
Condition(s)
- Name:
- SYNM-related disorder
- Synonyms:
- SYNM-related condition
- Identifiers:
Assertion and evidence details
Last Updated: May 19, 2024