NM_014209.4(ETV2):c.676C>T (p.Arg226Cys) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 15, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004191194.1
Allele description [Variation Report for NM_014209.4(ETV2):c.676C>T (p.Arg226Cys)]
NM_014209.4(ETV2):c.676C>T (p.Arg226Cys)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
PREDICTED: Rattus norvegicus NOP9 nucleolar protein (Nop9), transcript variant X...
PREDICTED: Rattus norvegicus NOP9 nucleolar protein (Nop9), transcript variant X1, mRNAgi|2678898661|ref|XM_063274131.1|Nucleotide
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Last Updated: Oct 8, 2024