NM_000251.3(MSH2):c.1387-20T>G AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000773308.2
Allele description [Variation Report for NM_000251.3(MSH2):c.1387-20T>G]
NM_000251.3(MSH2):c.1387-20T>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
-
Homo sapiens regucalcin (senescence marker protein-30) (RGN), transcript variant...
Homo sapiens regucalcin (senescence marker protein-30) (RGN), transcript variant 2, mRNAgi|23111020|ref|NM_152869.1|Nucleotide
-
Homo sapiens regucalcin (senescence marker protein-30), mRNA (cDNA clone MGC:877...
Homo sapiens regucalcin (senescence marker protein-30), mRNA (cDNA clone MGC:87766 IMAGE:6186669), complete cdsgi|49118182|gb|BC073173.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023