NM_006516.4(SLC2A1):c.392T>C (p.Val131Ala) AND Epilepsy, idiopathic generalized, susceptibility to, 12
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Apr 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002287482.4
Allele description [Variation Report for NM_006516.4(SLC2A1):c.392T>C (p.Val131Ala)]
NM_006516.4(SLC2A1):c.392T>C (p.Val131Ala)
Condition(s)
Assertion and evidence details
Last Updated: Jun 23, 2024