NM_000059.4(BRCA2):c.6560C>T (p.Pro2187Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (4 submissions)
- Last evaluated:
- Mar 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000129413.19
Allele description [Variation Report for NM_000059.4(BRCA2):c.6560C>T (p.Pro2187Leu)]
NM_000059.4(BRCA2):c.6560C>T (p.Pro2187Leu)
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 terminal nucleotidyltransferase 5A (Tent5a), mRNA
Rattus norvegicus terminal nucleotidyltransferase 5A (Tent5a), mRNAgi|157820522|ref|NM_001106844.1|Nucleotide
-
Mus musculus xylulokinase homolog (H. influenzae), mRNA (cDNA clone IMAGE:421174...
Mus musculus xylulokinase homolog (H. influenzae), mRNA (cDNA clone IMAGE:4211747), partial cdsgi|20071374|gb|BC026406.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 20, 2024