NM_004064.5(CDKN1B):c.394G>A (p.Asp132Asn) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 4, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002352722.2
Allele description [Variation Report for NM_004064.5(CDKN1B):c.394G>A (p.Asp132Asn)]
NM_004064.5(CDKN1B):c.394G>A (p.Asp132Asn)
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
-
UNVERIFIED: Cephaloleia erichsonii isolate BOFCR1712-15 cytochrome oxidase subun...
UNVERIFIED: Cephaloleia erichsonii isolate BOFCR1712-15 cytochrome oxidase subunit I-like (COI) gene, partial sequence; mitochondrialgi|982860152|gb|KU357497.1|Nucleotide
-
Homo sapiens TUB like protein 3 (TULP3), transcript variant 1, mRNA
Homo sapiens TUB like protein 3 (TULP3), transcript variant 1, mRNAgi|1519244494|ref|NM_003324.5|Nucleotide
-
L-arabinose regulatory protein [Expression vector pBAD18-Kan]
L-arabinose regulatory protein [Expression vector pBAD18-Kan]gi|2461860539|dbj|BDY34595.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024