NM_001571.6(IRF3):c.659T>C (p.Ile220Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 17, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004109736.1
Allele description [Variation Report for NM_001571.6(IRF3):c.659T>C (p.Ile220Thr)]
NM_001571.6(IRF3):c.659T>C (p.Ile220Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
serine/threonine-protein kinase tousled-like 2 isoform X13 [Homo sapiens]
serine/threonine-protein kinase tousled-like 2 isoform X13 [Homo sapiens]gi|2217309521|ref|XP_047291136.1|Protein
-
PREDICTED: Homo sapiens tousled like kinase 2 (TLK2), transcript variant X16, mR...
PREDICTED: Homo sapiens tousled like kinase 2 (TLK2), transcript variant X16, mRNAgi|2462552559|ref|XM_054314794.1|Nucleotide
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Last Updated: Sep 8, 2024