NM_024675.4(PALB2):c.3113+28C>T AND Hereditary breast ovarian cancer syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 19, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002226279.1
Allele description [Variation Report for NM_024675.4(PALB2):c.3113+28C>T]
NM_024675.4(PALB2):c.3113+28C>T
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
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LYR motif-containing protein 1 isoform 1 [Homo sapiens]
LYR motif-containing protein 1 isoform 1 [Homo sapiens]gi|1614230084|ref|NP_001356570.1|Protein
-
Homo sapiens glutaminase 2 (GLS2), transcript variant 4, mRNA; nuclear gene for ...
Homo sapiens glutaminase 2 (GLS2), transcript variant 4, mRNA; nuclear gene for mitochondrial productgi|1890334077|ref|NM_001280797.2|Nucleotide
-
Homo sapiens ATM interactor (ATMIN), transcript variant 1, mRNA
Homo sapiens ATM interactor (ATMIN), transcript variant 1, mRNAgi|1519246152|ref|NM_015251.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Jul 15, 2024