NM_001079802.2(FKTN):c.444C>T (p.Asp148=) AND Walker-Warburg congenital muscular dystrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000951807.9
Allele description [Variation Report for NM_001079802.2(FKTN):c.444C>T (p.Asp148=)]
NM_001079802.2(FKTN):c.444C>T (p.Asp148=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024