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
-
Rattus norvegicus strain BN/NHsdMcwi chromosome 5, GRCr8, whole genome shotgun s...
Rattus norvegicus strain BN/NHsdMcwi chromosome 5, GRCr8, whole genome shotgun sequencegi|2671914600|gnl|ASM:GCF_036323745 |ref|NC_086023.1||gpp|GPC_000020848.1||gnl|NCBI_GENOMES|157494Nucleotide
-
E3 ubiquitin-protein ligase TRIM13 [Mus musculus]
E3 ubiquitin-protein ligase TRIM13 [Mus musculus]gi|14149754|ref|NP_075722.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024