NM_000308.4(CTSA):c.33GCT[6] (p.Leu18_Leu19del) AND CTSA-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 3, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003979956.2
Allele description [Variation Report for NM_000308.4(CTSA):c.33GCT[6] (p.Leu18_Leu19del)]
NM_000308.4(CTSA):c.33GCT[6] (p.Leu18_Leu19del)
Condition(s)
- Name:
- CTSA-related disorder
- Synonyms:
- CTSA-related condition
- Identifiers:
-
Homo sapiens retinoic acid receptor gamma (RARG), transcript variant 5, mRNA
Homo sapiens retinoic acid receptor gamma (RARG), transcript variant 5, mRNAgi|1676320131|ref|NM_001243731.2|Nucleotide
-
Homo sapiens retinoic acid receptor, gamma, mRNA (cDNA clone IMAGE:5738222), con...
Homo sapiens retinoic acid receptor, gamma, mRNA (cDNA clone IMAGE:5738222), containing frame-shift errorsgi|40353036|gb|BC064524.1|Nucleotide
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Last Updated: Oct 26, 2024