NM_014915.3(ANKRD26):c.2679A>G (p.Gln893=) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Jun 21, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000253576.11
Allele description [Variation Report for NM_014915.3(ANKRD26):c.2679A>G (p.Gln893=)]
NM_014915.3(ANKRD26):c.2679A>G (p.Gln893=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024