NM_198281.3(GPRIN3):c.854C>T (p.Pro285Leu) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004256980.1
Allele description [Variation Report for NM_198281.3(GPRIN3):c.854C>T (p.Pro285Leu)]
NM_198281.3(GPRIN3):c.854C>T (p.Pro285Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 26, 2024