NM_000169.3(GLA):c.591C>T (p.Ser197=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 2, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002282164.2
Allele description [Variation Report for NM_000169.3(GLA):c.591C>T (p.Ser197=)]
NM_000169.3(GLA):c.591C>T (p.Ser197=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024