NM_001080414.4(CCDC88C):c.5066C>G (p.Pro1689Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002981501.2
Allele description [Variation Report for NM_001080414.4(CCDC88C):c.5066C>G (p.Pro1689Arg)]
NM_001080414.4(CCDC88C):c.5066C>G (p.Pro1689Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Actinoplanes abujensis NBRC 110796
Actinoplanes abujensis NBRC 110796biosample
-
CTAGE4 AND (alive[prop]) (4)
Gene
-
Cysteine-rich, acidic integral membrane protein [Melipona quadrifasciata]
Cysteine-rich, acidic integral membrane protein [Melipona quadrifasciata]gi|925679200|gb|KOX76149.1||gnl|WGS |WN51_11889Protein
-
nitrate reductase 1 subunit delta [Shigella flexneri 2a str. 301]
nitrate reductase 1 subunit delta [Shigella flexneri 2a str. 301]gi|24112625|ref|NP_707135.1|Protein
-
oligopeptide ABC transporter permease OppB [Shigella flexneri 2a str. 301]
oligopeptide ABC transporter permease OppB [Shigella flexneri 2a str. 301]gi|24112641|ref|NP_707151.1|Protein
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See more...Assertion and evidence details
Last Updated: May 1, 2024