NM_017736.5(THUMPD1):c.743G>T (p.Cys248Phe) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002694007.2
Allele description [Variation Report for NM_017736.5(THUMPD1):c.743G>T (p.Cys248Phe)]
NM_017736.5(THUMPD1):c.743G>T (p.Cys248Phe)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Screening for Anal Dysplasia and Cancer in Adults With HIV
Screening for Anal Dysplasia and Cancer in Adults With HIV
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Last Updated: May 1, 2024