NM_000213.5(ITGB4):c.3891G>T (p.Thr1297=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 20, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003704160.1
Allele description [Variation Report for NM_000213.5(ITGB4):c.3891G>T (p.Thr1297=)]
NM_000213.5(ITGB4):c.3891G>T (p.Thr1297=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 8, 2024