NM_019892.6(INPP5E):c.791G>A (p.Arg264His) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000251292.5
Allele description [Variation Report for NM_019892.6(INPP5E):c.791G>A (p.Arg264His)]
NM_019892.6(INPP5E):c.791G>A (p.Arg264His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Mar 10, 2024