NM_001165963.4(SCN1A):c.5882T>C (p.Ile1961Thr) AND Early infantile epileptic encephalopathy with suppression bursts
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 25, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001359104.7
Allele description
NM_001165963.4(SCN1A):c.5882T>C (p.Ile1961Thr)
Condition(s)
-
Homo sapiens cDNA clone IMAGE:40011687
Homo sapiens cDNA clone IMAGE:40011687gi|115304829|gb|BC122530.1|Nucleotide
-
Homo sapiens protein kinase C, alpha, mRNA (cDNA clone MGC:129901 IMAGE:40028308...
Homo sapiens protein kinase C, alpha, mRNA (cDNA clone MGC:129901 IMAGE:40028308), complete cdsgi|80479083|gb|BC109274.1|Nucleotide
-
Same Parent, Connectivity for PubChem Compound (Select 145005166) (3)
PubChem Compound
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024