NM_000059.4(BRCA2):c.201G>T (p.Arg67Ser) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 19, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002419559.2
Allele description [Variation Report for NM_000059.4(BRCA2):c.201G>T (p.Arg67Ser)]
NM_000059.4(BRCA2):c.201G>T (p.Arg67Ser)
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
-
Homo sapiens family with sequence similarity 83, member E, mRNA (cDNA clone MGC:...
Homo sapiens family with sequence similarity 83, member E, mRNA (cDNA clone MGC:138177 IMAGE:8327440), complete cdsgi|85567068|gb|BC111972.1|Nucleotide
-
Patellaria cenangiicola (0)
Taxonomy
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 1, 2024