NM_001199138.2(NLRC4):c.597C>G (p.Phe199Leu) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004493389.1
Allele description [Variation Report for NM_001199138.2(NLRC4):c.597C>G (p.Phe199Leu)]
NM_001199138.2(NLRC4):c.597C>G (p.Phe199Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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hypothetical protein SSSM5_072 [Synechococcus phage S-SSM5]
hypothetical protein SSSM5_072 [Synechococcus phage S-SSM5]gi|326784371|ref|YP_004324675.1|Protein
-
D-glycerate dehydrogenase [Fuscovulum ytuae]
D-glycerate dehydrogenase [Fuscovulum ytuae]gi|2500976872|gnl|PRJNA958438|QF092 0|gb|WGV17703.1|Protein
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The included studies in the updated review - Models and applications for measuri...
The included studies in the updated review - Models and applications for measuring the impact of health research: update of a systematic review for the Health Technology Assessment programme
-
Ndufa4 [Mastomys coucha]
Ndufa4 [Mastomys coucha]Gene ID:116098581Gene
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Last Updated: May 7, 2024