NM_000399.5(EGR2):c.764C>G (p.Thr255Ser) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 22, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003195284.2
Allele description [Variation Report for NM_000399.5(EGR2):c.764C>G (p.Thr255Ser)]
NM_000399.5(EGR2):c.764C>G (p.Thr255Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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ribosomal protein S16 (chloroplast) [Lotus japonicus]
ribosomal protein S16 (chloroplast) [Lotus japonicus]gi|13518446|ref|NP_084806.1|Protein
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Homo sapiens eukaryotic translation initiation factor 2D (EIF2D), transcript var...
Homo sapiens eukaryotic translation initiation factor 2D (EIF2D), transcript variant 2, mRNAgi|319918870|ref|NM_001201478.1|Nucleotide
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3530_1_83_1_A05.x_1 3530 - Full length cDNA library created by Invitrogen from m...
3530_1_83_1_A05.x_1 3530 - Full length cDNA library created by Invitrogen from multiple tissues Zea mays cDNA, mRNA sequencegi|37424948|gnl|dbEST|19975510|gb|C 08.1|Nucleotide
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Last Updated: May 1, 2024