NM_024867.4(SPEF2):c.935G>A (p.Arg312Gln) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003342442.2
Allele description [Variation Report for NM_024867.4(SPEF2):c.935G>A (p.Arg312Gln)]
NM_024867.4(SPEF2):c.935G>A (p.Arg312Gln)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
RNA-dependent RNA polymerase, partial [Coronavirus PREDICT_CoV-100]
RNA-dependent RNA polymerase, partial [Coronavirus PREDICT_CoV-100]gi|2243697019|gb|URC19495.1|Protein
-
RNA-dependent RNA polymerase, partial [Murine coronavirus]
RNA-dependent RNA polymerase, partial [Murine coronavirus]gi|2243704817|gb|URC20761.1|Protein
-
Aortic Arch Syndromes
Aortic Arch SyndromesConditions resulting from abnormalities in the arteries branching from the ASCENDING AORTA, the curved portion of the aorta. These syndromes are results of occlusion or abnorm...<br/>Year introduced: 1965MeSH
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See more...Assertion and evidence details
Last Updated: May 1, 2024