NM_000059.4(BRCA2):c.3902C>T (p.Thr1301Ile) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (2 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:
- RCV000773740.9
Allele description [Variation Report for NM_000059.4(BRCA2):c.3902C>T (p.Thr1301Ile)]
NM_000059.4(BRCA2):c.3902C>T (p.Thr1301Ile)
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
-
daa25b07.y1 NICHD_XGC_Lu1 Xenopus laevis cDNA clone IMAGE:4057284 5' similar to ...
daa25b07.y1 NICHD_XGC_Lu1 Xenopus laevis cDNA clone IMAGE:4057284 5' similar to TR:O43791 O43791 SPECKLE-TYPE PROTEIN SPOP, mRNA sequencegi|12694610|gnl|dbEST|7761834|gb|BG 1.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024