NM_000051.4(ATM):c.2040C>T (p.Phe680=) AND not specified
- Germline classification:
- Benign/Likely benign (4 submissions)
- Last evaluated:
- Feb 6, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000211972.7
Allele description [Variation Report for NM_000051.4(ATM):c.2040C>T (p.Phe680=)]
NM_000051.4(ATM):c.2040C>T (p.Phe680=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024