NM_198576.4(AGRN):c.4352C>T (p.Pro1451Leu) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Dec 23, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000243502.13
Allele description [Variation Report for NM_198576.4(AGRN):c.4352C>T (p.Pro1451Leu)]
NM_198576.4(AGRN):c.4352C>T (p.Pro1451Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 12, 2024