NM_004064.5(CDKN1B):c.442T>C (p.Cys148Arg) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 5, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002331501.2
Allele description [Variation Report for NM_004064.5(CDKN1B):c.442T>C (p.Cys148Arg)]
NM_004064.5(CDKN1B):c.442T>C (p.Cys148Arg)
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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UDP-glycosyltransferase family 37 member C1 [Drosophila melanogaster]
UDP-glycosyltransferase family 37 member C1 [Drosophila melanogaster]gi|2329048337|ref|NP_525007.2|Protein
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Homo sapiens olfactory receptor, family 2, subfamily AT, member 4, mRNA (cDNA cl...
Homo sapiens olfactory receptor, family 2, subfamily AT, member 4, mRNA (cDNA clone MGC:168573 IMAGE:9020950), complete cdsgi|223462747|gb|BC136958.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024