NM_001079802.2(FKTN):c.374G>C (p.Gly125Ala) AND Walker-Warburg congenital muscular dystrophy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 8, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001918560.3
Allele description [Variation Report for NM_001079802.2(FKTN):c.374G>C (p.Gly125Ala)]
NM_001079802.2(FKTN):c.374G>C (p.Gly125Ala)
Condition(s)
-
PIK3CG [Myotis davidii]
PIK3CG [Myotis davidii]Gene ID:102773870Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024