NM_001194998.2(CEP152):c.1598C>A (p.Pro533Gln) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003293885.2
Allele description [Variation Report for NM_001194998.2(CEP152):c.1598C>A (p.Pro533Gln)]
NM_001194998.2(CEP152):c.1598C>A (p.Pro533Gln)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
tumor protein D52 isoform X7 [Rattus norvegicus]
tumor protein D52 isoform X7 [Rattus norvegicus]gi|2678917463|ref|XP_063137612.1|Protein
-
Homo sapiens GPCR gene for putative G-protein coupled receptor, complete CDS, cl...
Homo sapiens GPCR gene for putative G-protein coupled receptor, complete CDS, clone:hGPCR32gi|20152291|dbj|AB083614.1|Nucleotide
-
translocation protein SEC63 homolog isoform X1 [Rattus norvegicus]
translocation protein SEC63 homolog isoform X1 [Rattus norvegicus]gi|564398265|ref|XP_006256632.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024