NM_000124.4(ERCC6):c.721C>T (p.Arg241Cys) AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jun 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001779750.7
Allele description [Variation Report for NM_000124.4(ERCC6):c.721C>T (p.Arg241Cys)]
NM_000124.4(ERCC6):c.721C>T (p.Arg241Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens GAR1 ribonucleoprotein (GAR1), transcript variant 2, mRNA
Homo sapiens GAR1 ribonucleoprotein (GAR1), transcript variant 2, mRNAgi|77812668|ref|NM_032993.2|Nucleotide
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Last Updated: Oct 8, 2024