NM_000208.4(INSR):c.1861+286_1861+287del AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001637505.3
Allele description [Variation Report for NM_000208.4(INSR):c.1861+286_1861+287del]
NM_000208.4(INSR):c.1861+286_1861+287del
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens serine/threonine kinase 19 (STK19), transcript variant 2, mRNA
Homo sapiens serine/threonine kinase 19 (STK19), transcript variant 2, mRNAgi|14602430|ref|NM_032454.1|Nucleotide
-
Homo sapiens zinc finger protein 683, mRNA (cDNA clone MGC:33414 IMAGE:4829037),...
Homo sapiens zinc finger protein 683, mRNA (cDNA clone MGC:33414 IMAGE:4829037), complete cdsgi|34192581|gb|BC028731.2|Nucleotide
-
Inclusion Bodies
Inclusion BodiesA generic term for any circumscribed mass of foreign (e.g., lead or viruses) or metabolically inactive materials (e.g., ceroid or MALLORY BODIES), within the cytoplasm or nucl...<br/>Year introduced: 1994MeSH
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Last Updated: Dec 24, 2023