NM_000029.4(AGT):c.803T>C (p.Met268Thr) AND not specified
- Germline classification:
- Benign (3 submissions)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000242838.9
Allele description [Variation Report for NM_000029.4(AGT):c.803T>C (p.Met268Thr)]
NM_000029.4(AGT):c.803T>C (p.Met268Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 15, 2024