NM_001079802.2(FKTN):c.166C>T (p.Arg56Cys) AND Walker-Warburg congenital muscular dystrophy
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000466034.20
Allele description [Variation Report for NM_001079802.2(FKTN):c.166C>T (p.Arg56Cys)]
NM_001079802.2(FKTN):c.166C>T (p.Arg56Cys)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024