NM_000314.8(PTEN):c.-836T>G AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 18, 2013
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000130962.1
Allele description [Variation Report for NM_000314.8(PTEN):c.-836T>G]
NM_000314.8(PTEN):c.-836T>G
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 speedy homolog A (Xenopus laevis) (SPDYA), transcript variant 2, mR...
Homo sapiens speedy homolog A (Xenopus laevis) (SPDYA), transcript variant 2, mRNAgi|60498968|ref|NM_182756.2|Nucleotide
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Uncultured bacterium clone UP_S_22 PAH dioxygenase large subunit (pahAc) gene, p...
Uncultured bacterium clone UP_S_22 PAH dioxygenase large subunit (pahAc) gene, partial cdsgi|87331869|gb|DQ325380.1|Nucleotide
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probable aminopeptidase NPEPL1 isoform 1 [Homo sapiens]
probable aminopeptidase NPEPL1 isoform 1 [Homo sapiens]gi|47155554|ref|NP_078939.3|Protein
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Last Updated: Dec 24, 2023