NM_001365536.1(SCN9A):c.3195C>T (p.Ser1065=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 27, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000118299.6
Allele description [Variation Report for NM_001365536.1(SCN9A):c.3195C>T (p.Ser1065=)]
NM_001365536.1(SCN9A):c.3195C>T (p.Ser1065=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
vacuolar protein sorting-associated protein 53 homolog isoform X8 [Homo sapiens]
vacuolar protein sorting-associated protein 53 homolog isoform X8 [Homo sapiens]gi|2462556290|ref|XP_054172587.1|Protein
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See more...Assertion and evidence details
Last Updated: Oct 26, 2024