NM_001330260.2(SCN8A):c.576C>T (p.Asp192=) AND Inborn genetic diseases
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Dec 31, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002312502.9
Allele description [Variation Report for NM_001330260.2(SCN8A):c.576C>T (p.Asp192=)]
NM_001330260.2(SCN8A):c.576C>T (p.Asp192=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
VP9, partial [Callinectes sapidus reovirus 1]
VP9, partial [Callinectes sapidus reovirus 1]gi|2449537567|gb|WDS83805.1|Protein
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024