NM_000051.4(ATM):c.2654T>C (p.Leu885Ser) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001016222.4
Allele description [Variation Report for NM_000051.4(ATM):c.2654T>C (p.Leu885Ser)]
NM_000051.4(ATM):c.2654T>C (p.Leu885Ser)
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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Rattus norvegicus ligand of numb-protein X 1 (Lnx1), mRNA
Rattus norvegicus ligand of numb-protein X 1 (Lnx1), mRNAgi|157821022|ref|NM_001108358.1|Nucleotide
-
Homo sapiens ATPase, class I, type 8B, member 4, mRNA (cDNA clone IMAGE:6668549)...
Homo sapiens ATPase, class I, type 8B, member 4, mRNA (cDNA clone IMAGE:6668549), partial cdsgi|34980823|gb|BC057236.1|Nucleotide
-
Mus musculus complement component 4B (Childo blood group), mRNA (cDNA clone IMAG...
Mus musculus complement component 4B (Childo blood group), mRNA (cDNA clone IMAGE:3583577)gi|15301511|gb|BC013237.1|Nucleotide
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cacna1ba [Clinocottus analis]
cacna1ba [Clinocottus analis]Gene ID:137801439Gene
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Last Updated: Sep 29, 2024