NM_001178015.2(SLC4A10):c.796C>T (p.Pro266Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002749291.2
Allele description [Variation Report for NM_001178015.2(SLC4A10):c.796C>T (p.Pro266Ser)]
NM_001178015.2(SLC4A10):c.796C>T (p.Pro266Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Related DataSets for GEO Profiles (Select 18391370) (1)
GEO DataSets
-
MyD88-deficient macrophage response to lipopolysaccharide and E. coli (dye swap)
MyD88-deficient macrophage response to lipopolysaccharide and E. coli (dye swap)Accession: GDS1706GEO DataSets
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See more...Assertion and evidence details
Last Updated: May 1, 2024