NM_020451.3(SELENON):c.1469G>A (p.Trp490Ter) AND not provided
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Apr 28, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000591683.6
Allele description [Variation Report for NM_020451.3(SELENON):c.1469G>A (p.Trp490Ter)]
NM_020451.3(SELENON):c.1469G>A (p.Trp490Ter)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024