NM_016138.5(COQ7):c.73+5A>G AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 28, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001908388.4
Allele description [Variation Report for NM_016138.5(COQ7):c.73+5A>G]
NM_016138.5(COQ7):c.73+5A>G
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
LOC127460392 [Homo sapiens]
LOC127460392 [Homo sapiens]Gene ID:127460392Gene
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Last Updated: Sep 29, 2024