NM_007194.4(CHEK2):c.1513T>A (p.Ser505Thr) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 7, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001193688.3
Allele description [Variation Report for NM_007194.4(CHEK2):c.1513T>A (p.Ser505Thr)]
NM_007194.4(CHEK2):c.1513T>A (p.Ser505Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024