NM_014140.4(SMARCAL1):c.423T>C (p.Tyr141=) AND not specified
- Germline classification:
- Benign (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000244412.6
Allele description [Variation Report for NM_014140.4(SMARCAL1):c.423T>C (p.Tyr141=)]
NM_014140.4(SMARCAL1):c.423T>C (p.Tyr141=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Oct 8, 2024