NM_000051.4(ATM):c.6828T>A (p.Phe2276Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 5, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001025693.11
Allele description [Variation Report for NM_000051.4(ATM):c.6828T>A (p.Phe2276Leu)]
NM_000051.4(ATM):c.6828T>A (p.Phe2276Leu)
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
-
Homo sapiens hypothetical protein MGC39820 (MGC39820), mRNA
Homo sapiens hypothetical protein MGC39820 (MGC39820), mRNAgi|27659733|ref|NM_173359.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 20, 2024