NM_000075.4(CDK4):c.823A>T (p.Met275Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000129910.7
Allele description [Variation Report for NM_000075.4(CDK4):c.823A>T (p.Met275Leu)]
NM_000075.4(CDK4):c.823A>T (p.Met275Leu)
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 coiled-coil domain containing 138 (CCDC138), transcript variant 8, ...
Homo sapiens coiled-coil domain containing 138 (CCDC138), transcript variant 8, mRNAgi|1890333404|ref|NM_001351549.2|Nucleotide
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meiotic central spindle, isoform A [Drosophila melanogaster]
meiotic central spindle, isoform A [Drosophila melanogaster]gi|17647627|ref|NP_524062.1|Protein
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Chain R, Photosystem II protein Y
Chain R, Photosystem II protein Ygi|728055573|pdb|4UB6|RProtein
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OSM oncostatin M [Homo sapiens]
OSM oncostatin M [Homo sapiens]Gene ID:5008Gene
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See more...Assertion and evidence details
Last Updated: Sep 1, 2024