NM_001184.4(ATR):c.7791G>A (p.Gln2597=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002407359.2
Allele description [Variation Report for NM_001184.4(ATR):c.7791G>A (p.Gln2597=)]
NM_001184.4(ATR):c.7791G>A (p.Gln2597=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
torsin-1A-interacting protein 2-like [Trichomycterus rosablanca]
torsin-1A-interacting protein 2-like [Trichomycterus rosablanca]gi|2673051474|ref|XP_062854483.1|Protein
-
SET domain-containing protein 4 isoform X2 [Homo sapiens]
SET domain-containing protein 4 isoform X2 [Homo sapiens]gi|2462582918|ref|XP_054180654.1|Protein
-
Homo sapiens ankyrin repeat-containing protein (ANKRD11) mRNA, complete cds
Homo sapiens ankyrin repeat-containing protein (ANKRD11) mRNA, complete cdsgi|38638916|gb|AY373756.1|Nucleotide
-
Pmfbp1 polyamine modulated factor 1 binding protein 1 [Mus musculus]
Pmfbp1 polyamine modulated factor 1 binding protein 1 [Mus musculus]Gene ID:56523Gene
-
56523[uid] AND (alive[prop]) (1)
Gene
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Last Updated: Sep 29, 2024