NM_001126049.2(KLLN):c.-956G>T AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 22, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002258808.8
Allele description [Variation Report for NM_001126049.2(KLLN):c.-956G>T]
NM_001126049.2(KLLN):c.-956G>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 nuclear factor of activated T-cells, cytoplasmic, calcineurin-depen...
Homo sapiens nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 2 (NFATC2), transcript variant 2, mRNAgi|75813623|ref|NM_173091.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Nov 10, 2024