NM_014319.5(LEMD3):c.907G>T (p.Gly303Cys) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 24, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000906602.6
Allele description [Variation Report for NM_014319.5(LEMD3):c.907G>T (p.Gly303Cys)]
NM_014319.5(LEMD3):c.907G>T (p.Gly303Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens
Homo sapiensRefSeq annotation of the human reference genome assemblyBioProject
-
BioProject Links for Nucleotide (Select 568801979) (1)
BioProject
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Last Updated: Feb 20, 2024