NM_018109.4(MTPAP):c.1054G>A (p.Ala352Thr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004507149.1
Allele description [Variation Report for NM_018109.4(MTPAP):c.1054G>A (p.Ala352Thr)]
NM_018109.4(MTPAP):c.1054G>A (p.Ala352Thr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Caenorhabditis elegans Negative Effect on Gut development (neg-1), mRNA
Caenorhabditis elegans Negative Effect on Gut development (neg-1), mRNAgi|1734333807|ref|NM_001269107.2|Nucleotide
-
RecName: Full=NKG2-C type II integral membrane protein; AltName: Full=CD159 anti...
RecName: Full=NKG2-C type II integral membrane protein; AltName: Full=CD159 antigen-like family member C; AltName: Full=NK cell receptor C; AltName: Full=NKG2-C-activating NK receptor; AltName: CD_antigen=CD159cgi|2245149901|sp|P26717.3|NKG2C_HUMProtein
-
Sporosarcina psychrophila NBRC 15381
Sporosarcina psychrophila NBRC 15381biosample
-
ML3
ML3biosample
-
Odobenus rosmarus rosmarus
Odobenus rosmarus rosmarusOdobenus rosmarus rosmarus Phenotype or GenotypeBioProject
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 7, 2024