NM_001122955.4(BSCL2):c.844G>A (p.Ala282Thr) AND not provided
- Germline classification:
- Uncertain significance (3 submissions)
- Last evaluated:
- Jan 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000994647.26
Allele description [Variation Report for NM_001122955.4(BSCL2):c.844G>A (p.Ala282Thr)]
NM_001122955.4(BSCL2):c.844G>A (p.Ala282Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024