NM_000051.4(ATM):c.8391T>C (p.Ser2797=) AND not specified
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jul 19, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000423464.12
Allele description [Variation Report for NM_000051.4(ATM):c.8391T>C (p.Ser2797=)]
NM_000051.4(ATM):c.8391T>C (p.Ser2797=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Feb 8, 2025