NM_000064.4(C3):c.3671G>A (p.Gly1224Asp) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- May 14, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001727686.5
Allele description [Variation Report for NM_000064.4(C3):c.3671G>A (p.Gly1224Asp)]
NM_000064.4(C3):c.3671G>A (p.Gly1224Asp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 11, 2024