NM_024680.4(E2F8):c.692T>C (p.Ile231Thr) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 14, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000879342.4
Allele description [Variation Report for NM_024680.4(E2F8):c.692T>C (p.Ile231Thr)]
NM_024680.4(E2F8):c.692T>C (p.Ile231Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens Wnt family member 3A (WNT3A), mRNA
Homo sapiens Wnt family member 3A (WNT3A), mRNAgi|1519242293|ref|NM_033131.4|Nucleotide
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Last Updated: Sep 29, 2024