NM_016373.4(WWOX):c.876T>G (p.Ala292=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Sep 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001703730.7
Allele description [Variation Report for NM_016373.4(WWOX):c.876T>G (p.Ala292=)]
NM_016373.4(WWOX):c.876T>G (p.Ala292=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 12, 2024