NM_000466.3(PEX1):c.472+5G>A AND Zellweger spectrum disorders
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Oct 6, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001210774.10
Allele description [Variation Report for NM_000466.3(PEX1):c.472+5G>A]
NM_000466.3(PEX1):c.472+5G>A
Condition(s)
-
Homo sapiens chromosome 17 open reading frame 102, mRNA (cDNA clone MGC:164873 I...
Homo sapiens chromosome 17 open reading frame 102, mRNA (cDNA clone MGC:164873 IMAGE:40148022), complete cdsgi|148753295|gb|BC142651.1|Nucleotide
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Last Updated: Sep 29, 2024