NM_147127.5(EVC2):c.1749T>C (p.Ser583=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003802578.1
Allele description [Variation Report for NM_147127.5(EVC2):c.1749T>C (p.Ser583=)]
NM_147127.5(EVC2):c.1749T>C (p.Ser583=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024