NM_014795.4(ZEB2):c.2325G>A (p.Leu775=) AND Mowat-Wilson syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 26, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001505358.13
Allele description [Variation Report for NM_014795.4(ZEB2):c.2325G>A (p.Leu775=)]
NM_014795.4(ZEB2):c.2325G>A (p.Leu775=)
Condition(s)
-
Homo sapiens latexin mRNA, complete cds
Homo sapiens latexin mRNA, complete cdsgi|9082320|gb|AF282626.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024