NM_213599.3(ANO5):c.276A>G (p.Lys92=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 17, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000321766.3
Allele description [Variation Report for NM_213599.3(ANO5):c.276A>G (p.Lys92=)]
NM_213599.3(ANO5):c.276A>G (p.Lys92=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024