NM_001159699.2(FHL1):c.379+7C>T AND X-linked myopathy with postural muscle atrophy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 13, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002599469.2
Allele description [Variation Report for NM_001159699.2(FHL1):c.379+7C>T]
NM_001159699.2(FHL1):c.379+7C>T
Condition(s)
-
neural cell adhesion molecule L1-like protein isoform X2 [Homo sapiens]
neural cell adhesion molecule L1-like protein isoform X2 [Homo sapiens]gi|1034630797|ref|XP_016861060.1|Protein
-
Homo sapiens BAC clone RP11-746I5 from 2, complete sequence
Homo sapiens BAC clone RP11-746I5 from 2, complete sequencegi|18693586|gb|AC093162.5||gnl|wugs 1-746I5Nucleotide
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See more...Assertion and evidence details
Last Updated: Feb 28, 2024