NM_020812.4(DOCK6):c.810C>T (p.Phe270=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 21, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000904322.6
Allele description [Variation Report for NM_020812.4(DOCK6):c.810C>T (p.Phe270=)]
NM_020812.4(DOCK6):c.810C>T (p.Phe270=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 12, 2024