NM_001122955.4(BSCL2):c.744C>T (p.Tyr248=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003395880.8
Allele description [Variation Report for NM_001122955.4(BSCL2):c.744C>T (p.Tyr248=)]
NM_001122955.4(BSCL2):c.744C>T (p.Tyr248=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Aug 4, 2024