NM_000059.4(BRCA2):c.8090G>T (p.Ser2697Ile) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 11, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002419440.2
Allele description [Variation Report for NM_000059.4(BRCA2):c.8090G>T (p.Ser2697Ile)]
NM_000059.4(BRCA2):c.8090G>T (p.Ser2697Ile)
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 myosin IF (MYO1F), mRNA
Homo sapiens myosin IF (MYO1F), mRNAgi|24307944|ref|NM_012335.1|Nucleotide
-
Homo sapiens LUC7-like (S. cerevisiae), mRNA (cDNA clone MGC:988 IMAGE:3536109),...
Homo sapiens LUC7-like (S. cerevisiae), mRNA (cDNA clone MGC:988 IMAGE:3536109), complete cdsgi|13112036|gb|BC003194.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 1, 2024