NM_007294.4(BRCA1):c.*13A>G AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 23, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000583307.5
Allele description [Variation Report for NM_007294.4(BRCA1):c.*13A>G]
NM_007294.4(BRCA1):c.*13A>G
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
-
PREDICTED: Homo sapiens meiotic double-stranded break formation protein 1 (MEI1)...
PREDICTED: Homo sapiens meiotic double-stranded break formation protein 1 (MEI1), transcript variant X4, mRNAgi|2217339013|ref|XM_017028633.3|Nucleotide
-
55 kDa erythrocyte membrane protein isoform 3 [Homo sapiens]
55 kDa erythrocyte membrane protein isoform 3 [Homo sapiens]gi|262118259|ref|NP_001159933.1|Protein
-
PREDICTED: Homo sapiens meiotic double-stranded break formation protein 1 (MEI1)...
PREDICTED: Homo sapiens meiotic double-stranded break formation protein 1 (MEI1), transcript variant X1, mRNAgi|2217339010|ref|XM_011529945.4|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023