NM_001567.4(INPPL1):c.879A>G (p.Ala293=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003692653.2
Allele description [Variation Report for NM_001567.4(INPPL1):c.879A>G (p.Ala293=)]
NM_001567.4(INPPL1):c.879A>G (p.Ala293=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024