NM_003575.4(ZNF282):c.1414A>T (p.Thr472Ser) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004270381.1
Allele description [Variation Report for NM_003575.4(ZNF282):c.1414A>T (p.Thr472Ser)]
NM_003575.4(ZNF282):c.1414A>T (p.Thr472Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Homo sapiens chimerin 2 (CHN2), transcript variant X3, mRNA
PREDICTED: Homo sapiens chimerin 2 (CHN2), transcript variant X3, mRNAgi|2217365480|ref|XM_017011722.2|Nucleotide
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Last Updated: Oct 13, 2024