NM_016604.4(KDM3B):c.3493G>A (p.Gly1165Arg) AND KDM3B-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003410449.4
Allele description [Variation Report for NM_016604.4(KDM3B):c.3493G>A (p.Gly1165Arg)]
NM_016604.4(KDM3B):c.3493G>A (p.Gly1165Arg)
Condition(s)
- Name:
- KDM3B-related disorder
- Synonyms:
- KDM3B-related condition
- Identifiers:
-
Homo sapiens golgin A6 family like 17, pseudogene (GOLGA6L17P), non-coding RNA
Homo sapiens golgin A6 family like 17, pseudogene (GOLGA6L17P), non-coding RNAgi|611435035|ref|NR_111962.1|Nucleotide
-
Monocercomonoides exilis uncharacterized protein (MONOS_18517), partial mRNA
Monocercomonoides exilis uncharacterized protein (MONOS_18517), partial mRNAgi|2794979803|ref|XM_067871544.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 26, 2024