NM_198152.5(UTS2B):c.-665+470_-665+471del AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Sep 2, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001695549.1
Allele description [Variation Report for NM_198152.5(UTS2B):c.-665+470_-665+471del]
NM_198152.5(UTS2B):c.-665+470_-665+471del
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023