NM_016604.4(KDM3B):c.1720G>A (p.Val574Ile) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 23, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004634260.1
Allele description [Variation Report for NM_016604.4(KDM3B):c.1720G>A (p.Val574Ile)]
NM_016604.4(KDM3B):c.1720G>A (p.Val574Ile)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
polyprotein, partial [Hepacivirus hominis]
polyprotein, partial [Hepacivirus hominis]gi|338832385|gb|AEJ18053.1|Protein
-
AGENCOURT_7984679 NIH_MGC_71 Homo sapiens cDNA clone IMAGE:6174899 5', mRNA sequ...
AGENCOURT_7984679 NIH_MGC_71 Homo sapiens cDNA clone IMAGE:6174899 5', mRNA sequencegi|22681836|gnl|dbEST|13441848|gb|B 52.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Oct 20, 2024