NM_020451.3(SELENON):c.550G>C (p.Ala184Pro) AND SEPN1-Related Disorders
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000351042.5
Allele description [Variation Report for NM_020451.3(SELENON):c.550G>C (p.Ala184Pro)]
NM_020451.3(SELENON):c.550G>C (p.Ala184Pro)
Condition(s)
- Name:
- SEPN1-Related Disorders
- Identifiers:
- MedGen: CN239420
Assertion and evidence details
Last Updated: Mar 16, 2024