NM_198576.4(AGRN):c.4740C>T (p.Arg1580=) AND not specified
- Germline classification:
- Benign (4 submissions)
- Last evaluated:
- Aug 1, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000116273.15
Allele description [Variation Report for NM_198576.4(AGRN):c.4740C>T (p.Arg1580=)]
NM_198576.4(AGRN):c.4740C>T (p.Arg1580=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
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Last Updated: Sep 29, 2024