NM_138773.4(SLC25A46):c.1196A>G (p.His399Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002338594.2
Allele description [Variation Report for NM_138773.4(SLC25A46):c.1196A>G (p.His399Arg)]
NM_138773.4(SLC25A46):c.1196A>G (p.His399Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Clostridium manihotivorum strain CT4 16S ribosomal RNA, partial sequence
Clostridium manihotivorum strain CT4 16S ribosomal RNA, partial sequencegi|2221405546|gnl|REF_SSU16S|CP0257 4164-265691|ref|NR_175571.1|Nucleotide
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Seinonella peptonophila strain KCTC 9740 16S ribosomal RNA, partial sequence
Seinonella peptonophila strain KCTC 9740 16S ribosomal RNA, partial sequencegi|219857418|ref|NR_025006.1|Nucleotide
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TR34_RS08145 [Rodentibacter pneumotropicus]
TR34_RS08145 [Rodentibacter pneumotropicus]Gene ID:61267583Gene
-
Peritoneal Dialysis
Peritoneal DialysisDialysis fluid being introduced into and removed from the peritoneal cavity as either a continuous or an intermittent procedure.<br/>Year introduced: 1966(1964)MeSH
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Last Updated: May 1, 2024