NM_005911.6(MAT2A):c.406-19G>A AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Aug 10, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000436861.2
Allele description [Variation Report for NM_005911.6(MAT2A):c.406-19G>A]
NM_005911.6(MAT2A):c.406-19G>A
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 28, 2024