NM_203447.3(DOCK8):c.2383G>C (p.Val795Leu) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 5, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000859762.1
Allele description
NM_203447.3(DOCK8):c.2383G>C (p.Val795Leu)
Condition(s)
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 18, 2020