NM_001130173.2(MYB):c.214-10_214-7del AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 19, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000888993.3
Allele description [Variation Report for NM_001130173.2(MYB):c.214-10_214-7del]
NM_001130173.2(MYB):c.214-10_214-7del
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022