NM_030665.4(RAI1):c.109G>A (p.Gly37Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 13, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000502371.13
Allele description [Variation Report for NM_030665.4(RAI1):c.109G>A (p.Gly37Arg)]
NM_030665.4(RAI1):c.109G>A (p.Gly37Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 15, 2024