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
-
unnamed protein product [Homo sapiens]
unnamed protein product [Homo sapiens]gi|194386794|dbj|BAG61207.1|Protein
-
Rhodopseudomonas sp. P531(13) 16S ribosomal RNA gene, partial sequence
Rhodopseudomonas sp. P531(13) 16S ribosomal RNA gene, partial sequencegi|944383067|gb|GU370120.2|Nucleotide
-
Chain BK, Nascent chain
Chain BK, Nascent chaingi|2790389733|pdb|9F1D|BKProtein
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Last Updated: May 7, 2024