NM_018303.6(EXOC2):c.1632C>T (p.Ser544=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003428749.8
Allele description
NM_018303.6(EXOC2):c.1632C>T (p.Ser544=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024