NM_017635.5(KMT5B):c.2162G>A (p.Arg721His) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 5, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000623268.2
Allele description [Variation Report for NM_017635.5(KMT5B):c.2162G>A (p.Arg721His)]
NM_017635.5(KMT5B):c.2162G>A (p.Arg721His)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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BioProject Links for Nucleotide (Select 2577911603) (1)
BioProject
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BioProject Links for Nucleotide (Select 2662968854) (1)
BioProject
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BioProject Links for Protein (Select 2662968315) (1)
BioProject
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Apis cerana cerana
Apis cerana ceranaApis cerana cerana Transcriptome or Gene expressionBioProject
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Last Updated: Jan 7, 2023