NM_015076.5(CDK19):c.941A>G (p.Lys314Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003351986.2
Allele description [Variation Report for NM_015076.5(CDK19):c.941A>G (p.Lys314Arg)]
NM_015076.5(CDK19):c.941A>G (p.Lys314Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
GSE55793[Accession] (12)
GEO DataSets
-
T-cell receptor alpha chain, partial [Homo sapiens]
T-cell receptor alpha chain, partial [Homo sapiens]gi|338717|gb|AAA36667.1|Protein
-
Homo sapiens cDNA clone IMAGE:40148875, with apparent retained intron
Homo sapiens cDNA clone IMAGE:40148875, with apparent retained introngi|148753301|gb|BC142721.1|Nucleotide
-
carbamate kinase [Pragia fontium]
carbamate kinase [Pragia fontium]gi|836631511|ref|WP_047781230.1|Protein
-
Penicillium brevicompactum isolate PM15 beta-tubulin (benA) gene, partial cds
Penicillium brevicompactum isolate PM15 beta-tubulin (benA) gene, partial cdsgi|2449181486|gb|ON155598.1|Nucleotide
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Last Updated: May 1, 2024