NM_181836.6(TMED7):c.438+12_438+13dup AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002587207.3
Allele description [Variation Report for NM_181836.6(TMED7):c.438+12_438+13dup]
NM_181836.6(TMED7):c.438+12_438+13dup
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024