NM_000251.3(MSH2):c.76A>C (p.Met26Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 11, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000214711.3
Allele description [Variation Report for NM_000251.3(MSH2):c.76A>C (p.Met26Leu)]
NM_000251.3(MSH2):c.76A>C (p.Met26Leu)
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
-
Candida albicans SC5314 chromosome R, complete sequence
Candida albicans SC5314 chromosome R, complete sequencegi|1111963364|ref|NC_032096.1||gnl| CF_000182965.3|RNucleotide
-
Homo sapiens retinoschisin 1 (RS1), RefSeqGene on chromosome X
Homo sapiens retinoschisin 1 (RS1), RefSeqGene on chromosome Xgi|209417926|ref|NG_008659.1|Nucleotide
-
Mus musculus 3-ketodihydrosphingosine reductase (Kdsr), transcript variant 1, mR...
Mus musculus 3-ketodihydrosphingosine reductase (Kdsr), transcript variant 1, mRNAgi|169234751|ref|NM_027534.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024