NM_003153.5(STAT6):c.754A>C (p.Lys252Gln) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003275920.2
Allele description [Variation Report for NM_003153.5(STAT6):c.754A>C (p.Lys252Gln)]
NM_003153.5(STAT6):c.754A>C (p.Lys252Gln)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Gene Links for GEO Profiles (Select 109391206) (1)
Gene
-
LOC101928277 [Homo sapiens]
LOC101928277 [Homo sapiens]Gene ID:101928277Gene
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Last Updated: May 1, 2024