NM_020631.6(PLEKHG5):c.1469A>G (p.Lys490Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002395174.2
Allele description [Variation Report for NM_020631.6(PLEKHG5):c.1469A>G (p.Lys490Arg)]
NM_020631.6(PLEKHG5):c.1469A>G (p.Lys490Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
protein kinase C iota, partial [Raphicerus melanotis]
protein kinase C iota, partial [Raphicerus melanotis]gi|14572757|gb|AAK67779.1|Protein
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Entamoebidae sp. isolate ZOTU3104 18S ribosomal RNA gene, partial sequence
Entamoebidae sp. isolate ZOTU3104 18S ribosomal RNA gene, partial sequencegi|1594499408|gb|MH623070.1|Nucleotide
-
Taxonomy Links for GEO Profiles (Select 111836210) (1)
Taxonomy
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Last Updated: May 1, 2024