NM_000059.4(BRCA2):c.4278A>G (p.Thr1426=) AND Hereditary breast ovarian cancer syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 13, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002061765.6
Allele description [Variation Report for NM_000059.4(BRCA2):c.4278A>G (p.Thr1426=)]
NM_000059.4(BRCA2):c.4278A>G (p.Thr1426=)
Condition(s)
- Name:
- Hereditary breast ovarian cancer syndrome
- Synonyms:
- Hereditary breast and ovarian cancer syndrome; Hereditary breast and ovarian cancer; Hereditary breast and ovarian cancer syndrome (HBOC); See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0003582; MeSH: D061325; MedGen: C0677776; Orphanet: 145
-
Alpha proteobacterium IMCC10422 16S ribosomal RNA gene, partial sequence
Alpha proteobacterium IMCC10422 16S ribosomal RNA gene, partial sequencegi|220061865|gb|FJ532495.1|Nucleotide
-
Homo sapiens cDNA FLJ76078 complete cds
Homo sapiens cDNA FLJ76078 complete cdsgi|158261578|dbj|AK290278.1|Nucleotide
-
6p23 (56)
OMIM
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 1, 2024