NM_020812.4(DOCK6):c.5691G>A (p.Thr1897=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002662461.2
Allele description [Variation Report for NM_020812.4(DOCK6):c.5691G>A (p.Thr1897=)]
NM_020812.4(DOCK6):c.5691G>A (p.Thr1897=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 28, 2024