NM_006662.3(SRCAP):c.588C>T (p.Ser196=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003426654.5
Allele description [Variation Report for NM_006662.3(SRCAP):c.588C>T (p.Ser196=)]
NM_006662.3(SRCAP):c.588C>T (p.Ser196=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 12, 2024