NM_001384140.1(PCDH15):c.5160TGA[2] (p.Asp1722del) AND Usher syndrome type 1F
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 2, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000673742.1
Allele description [Variation Report for NM_001384140.1(PCDH15):c.5160TGA[2] (p.Asp1722del)]
NM_001384140.1(PCDH15):c.5160TGA[2] (p.Asp1722del)
Condition(s)
-
Homo sapiens zinc finger protein 668 (ZNF668), transcript variant 3, mRNA
Homo sapiens zinc finger protein 668 (ZNF668), transcript variant 3, mRNAgi|1890342071|ref|NM_001172669.2|Nucleotide
-
Rattus norvegicus X-linked myotubular myopathy gene 1, mRNA (cDNA clone IMAGE:71...
Rattus norvegicus X-linked myotubular myopathy gene 1, mRNA (cDNA clone IMAGE:7112710), partial cdsgi|50925902|gb|BC079400.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Apr 23, 2022