NM_024867.4(SPEF2):c.605G>A (p.Arg202Gln) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003348448.2
Allele description [Variation Report for NM_024867.4(SPEF2):c.605G>A (p.Arg202Gln)]
NM_024867.4(SPEF2):c.605G>A (p.Arg202Gln)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens TNF receptor superfamily member 13C (TNFRSF13C), mRNA
Homo sapiens TNF receptor superfamily member 13C (TNFRSF13C), mRNAgi|169808386|ref|NM_052945.3|Nucleotide
-
translation elongation factor 1-alpha, partial [Yamadazyma scolyti]
translation elongation factor 1-alpha, partial [Yamadazyma scolyti]gi|390195298|gb|AFL69898.1|Protein
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Last Updated: May 1, 2024