NM_000171.4(GLRA1):c.1032A>G (p.Arg344=) AND Hyperekplexia 1
- Germline classification:
- 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:
- RCV000878107.7
Allele description [Variation Report for NM_000171.4(GLRA1):c.1032A>G (p.Arg344=)]
NM_000171.4(GLRA1):c.1032A>G (p.Arg344=)
Condition(s)
- Name:
- Hyperekplexia 1 (STHE)
- Synonyms:
- Startle disease, familial; Startle reaction, exaggerated; Stiff-baby syndrome; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0007868; MedGen: C4551954; Orphanet: 3197; OMIM: 149400
Assertion and evidence details
Last Updated: Mar 5, 2024