NM_022124.6(CDH23):c.3462C>A (p.Val1154=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003574604.1
Allele description [Variation Report for NM_022124.6(CDH23):c.3462C>A (p.Val1154=)]
NM_022124.6(CDH23):c.3462C>A (p.Val1154=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens CUGBP Elav-like family member 1 (CELF1), transcript variant 9, mRNA
Homo sapiens CUGBP Elav-like family member 1 (CELF1), transcript variant 9, mRNAgi|1775678300|ref|NM_001376371.1|Nucleotide
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"Institute of Human Genetics, University of Leipzig Medical Cente... (1)
"Institute of Human Genetics, University of Leipzig Medical Center"[submitter] AND "VPS13C"[gene]SearchClinVar
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See more...Assertion and evidence details
Last Updated: Jun 2, 2024