NM_001329943.3(KIAA0586):c.261G>T (p.Val87=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002999882.2
Allele description [Variation Report for NM_001329943.3(KIAA0586):c.261G>T (p.Val87=)]
NM_001329943.3(KIAA0586):c.261G>T (p.Val87=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024