NM_016604.4(KDM3B):c.1695C>G (p.Ser565Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 2, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004409048.1
Allele description [Variation Report for NM_016604.4(KDM3B):c.1695C>G (p.Ser565Arg)]
NM_016604.4(KDM3B):c.1695C>G (p.Ser565Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
chymotrypsinogen B precursor [Mus musculus]
chymotrypsinogen B precursor [Mus musculus]gi|255522937|ref|NP_079859.2|Protein
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Synthetic construct clone IMAGE:100003953; FLH171085.01X; RZPDo839E11100D interf...
Synthetic construct clone IMAGE:100003953; FLH171085.01X; RZPDo839E11100D interferon (alpha, beta and omega) receptor 1 (IFNAR1) gene, encodes complete proteingi|123980839|gb|DQ891323.2|Nucleotide
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chymotrypsinogen B1, isoform CRA_b, partial [Mus musculus]
chymotrypsinogen B1, isoform CRA_b, partial [Mus musculus]gi|148679565|gb|EDL11512.1||gnl|WGS |mCP98223Protein
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unnamed protein product [Mus musculus]
unnamed protein product [Mus musculus]gi|12841520|dbj|BAB25241.1|Protein
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Last Updated: May 7, 2024