NM_007194.4(CHEK2):c.1343T>G (p.Ile448Ser) AND not specified
- Germline classification:
- Benign (5 submissions)
- Last evaluated:
- Aug 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000120559.16
Allele description [Variation Report for NM_007194.4(CHEK2):c.1343T>G (p.Ile448Ser)]
NM_007194.4(CHEK2):c.1343T>G (p.Ile448Ser)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Aug 11, 2024