NM_018139.3(DNAAF2):c.1406G>A (p.Cys469Tyr) AND not specified
- Germline classification:
- Benign/Likely benign (2 submissions)
- Last evaluated:
- Apr 13, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000253232.8
Allele description [Variation Report for NM_018139.3(DNAAF2):c.1406G>A (p.Cys469Tyr)]
NM_018139.3(DNAAF2):c.1406G>A (p.Cys469Tyr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 12, 2024