NM_000404.4(GLB1):c.1285C>T (p.Pro429Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003482247.1
Allele description [Variation Report for NM_000404.4(GLB1):c.1285C>T (p.Pro429Ser)]
NM_000404.4(GLB1):c.1285C>T (p.Pro429Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024