NM_002485.5(NBN):c.2187A>T (p.Val729=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 21, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001014698.3
Allele description [Variation Report for NM_002485.5(NBN):c.2187A>T (p.Val729=)]
NM_002485.5(NBN):c.2187A>T (p.Val729=)
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
-
nsv1001715 (0)
Biocollections
-
Chain B, EPIDIDYMAL RETINOIC ACID-BINDING PROTEIN
Chain B, EPIDIDYMAL RETINOIC ACID-BINDING PROTEINgi|576102|pdb|1EPA|BProtein
-
Rattus norvegicus similar to hypothetical protein, mRNA (cDNA clone MGC:112833 I...
Rattus norvegicus similar to hypothetical protein, mRNA (cDNA clone MGC:112833 IMAGE:7375621), complete cdsgi|68534284|gb|BC098792.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024