NM_001032221.6(STXBP1):c.87+19T>C AND Developmental and epileptic encephalopathy, 4
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003619151.1
Allele description [Variation Report for NM_001032221.6(STXBP1):c.87+19T>C]
NM_001032221.6(STXBP1):c.87+19T>C
Condition(s)
-
immunoglobulin superfamily DCC subclass member 3 isoform X1 [Homo sapiens]
immunoglobulin superfamily DCC subclass member 3 isoform X1 [Homo sapiens]gi|2462546808|ref|XP_054235232.1|Protein
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Last Updated: Feb 28, 2024