NM_000335.5(SCN5A):c.5882C>T (p.Pro1961Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 16, 2012
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000041634.15
Allele description [Variation Report for NM_000335.5(SCN5A):c.5882C>T (p.Pro1961Leu)]
NM_000335.5(SCN5A):c.5882C>T (p.Pro1961Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
phosphoglycerate mutase 1 (brain), isoform CRA_d [Homo sapiens]
phosphoglycerate mutase 1 (brain), isoform CRA_d [Homo sapiens]gi|119570326|gb|EAW49941.1||gnl|WGS |hCP1897299Protein
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Last Updated: Oct 26, 2024