NM_000051.4(ATM):c.2151G>C (p.Arg717=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Oct 28, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000581454.5
Allele description [Variation Report for NM_000051.4(ATM):c.2151G>C (p.Arg717=)]
NM_000051.4(ATM):c.2151G>C (p.Arg717=)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
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Last Updated: Sep 29, 2024