NM_001330260.2(SCN8A):c.141C>T (p.Asp47=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 21, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002312599.9
Allele description [Variation Report for NM_001330260.2(SCN8A):c.141C>T (p.Asp47=)]
NM_001330260.2(SCN8A):c.141C>T (p.Asp47=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Pyrrosia subfurfuracea voucher 041501, Wei XP rps4 pseudogene and rps4-trnS inte...
Pyrrosia subfurfuracea voucher 041501, Wei XP rps4 pseudogene and rps4-trnS intergenic spacer, partial sequence; chloroplastgi|1254403769|gb|KY633176.1|Nucleotide
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Last Updated: Oct 8, 2024