NM_000548.5(TSC2):c.5260-13C>T AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 8, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002258301.2
Allele description [Variation Report for NM_000548.5(TSC2):c.5260-13C>T]
NM_000548.5(TSC2):c.5260-13C>T
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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Homo sapiens 2'-5'-oligoadenylate synthetase-like (OASL), transcript variant 2, mRNAgi|38016929|ref|NM_198213.1|Nucleotide
-
Homo sapiens 2'-5'-oligoadenylate synthetase-like, mRNA (cDNA clone MGC:151017 I...
Homo sapiens 2'-5'-oligoadenylate synthetase-like, mRNA (cDNA clone MGC:151017 IMAGE:40125959), complete cdsgi|109658903|gb|BC117408.1|Nucleotide
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Last Updated: Sep 29, 2024