NM_001382273.1(TNK2):c.1494C>T (p.Ser498=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002966781.2
Allele description [Variation Report for NM_001382273.1(TNK2):c.1494C>T (p.Ser498=)]
NM_001382273.1(TNK2):c.1494C>T (p.Ser498=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024