NM_006516.4(SLC2A1):c.798C>T (p.Pro266=) AND Epilepsy, idiopathic generalized, susceptibility to, 12
- Germline classification:
- Likely benign (1 submission)
- 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:
- RCV003446629.1
Allele description [Variation Report for NM_006516.4(SLC2A1):c.798C>T (p.Pro266=)]
NM_006516.4(SLC2A1):c.798C>T (p.Pro266=)
Condition(s)
-
RRS1-DT RRS1 divergent transcript [Homo sapiens]
RRS1-DT RRS1 divergent transcript [Homo sapiens]Gene ID:100505676Gene
-
Gene Links for GEO Profiles (Select 86166379) (1)
Gene
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Last Updated: Mar 5, 2024