NM_000335.5(SCN5A):c.856G>T (p.Ala286Ser) AND SCN5A-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004537263.2
Allele description [Variation Report for NM_000335.5(SCN5A):c.856G>T (p.Ala286Ser)]
NM_000335.5(SCN5A):c.856G>T (p.Ala286Ser)
Condition(s)
- Name:
- SCN5A-related disorder
- Identifiers:
-
Homo sapiens retinol binding protein 5, cellular, mRNA (cDNA clone MGC:32522 IMA...
Homo sapiens retinol binding protein 5, cellular, mRNA (cDNA clone MGC:32522 IMAGE:4613026), complete cdsgi|20810176|gb|BC029355.1|Nucleotide
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Last Updated: Oct 13, 2024