NM_178862.3(STT3B):c.2142T>C (p.Asn714=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 20, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000615881.1
Allele description [Variation Report for NM_178862.3(STT3B):c.2142T>C (p.Asn714=)]
NM_178862.3(STT3B):c.2142T>C (p.Asn714=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Apr 23, 2022