NM_000702.4(ATP1A2):c.1461+5G>A AND not provided
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Sep 13, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001698235.12
Allele description [Variation Report for NM_000702.4(ATP1A2):c.1461+5G>A]
NM_000702.4(ATP1A2):c.1461+5G>A
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens ERCC excision repair 2, TFIIH core complex helicase subunit (ERCC2)...
Homo sapiens ERCC excision repair 2, TFIIH core complex helicase subunit (ERCC2), transcript variant 2, mRNAgi|1890283112|ref|NM_001130867.2|Nucleotide
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Last Updated: Nov 10, 2024