NM_001371727.1(GABRB2):c.896T>G (p.Ile299Ser) AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Apr 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000479130.1
Allele description [Variation Report for NM_001371727.1(GABRB2):c.896T>G (p.Ile299Ser)]
NM_001371727.1(GABRB2):c.896T>G (p.Ile299Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 23, 2022