NM_031485.4(GRWD1):c.859C>T (p.Arg287Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004097274.1
Allele description [Variation Report for NM_031485.4(GRWD1):c.859C>T (p.Arg287Cys)]
NM_031485.4(GRWD1):c.859C>T (p.Arg287Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jun 2, 2024