NM_001165963.4(SCN1A):c.5882T>C (p.Ile1961Thr) AND Generalized epilepsy with febrile seizures plus, type 2
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 23, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000678302.3
Allele description [Variation Report for NM_001165963.4(SCN1A):c.5882T>C (p.Ile1961Thr)]
NM_001165963.4(SCN1A):c.5882T>C (p.Ile1961Thr)
Condition(s)
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Homo sapiens killer cell lectin-like receptor subfamily C, member 1, mRNA (cDNA ...
Homo sapiens killer cell lectin-like receptor subfamily C, member 1, mRNA (cDNA clone MGC:13374 IMAGE:4042168), complete cdsgi|15214825|gb|BC012550.1|Nucleotide
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Adverse Event Associated with the Gastrointestinal System
Adverse Event Associated with the Gastrointestinal SystemMedGen
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Last Updated: Sep 29, 2024