NM_000251.3(MSH2):c.71A>G (p.Gln24Arg) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001179994.3
Allele description [Variation Report for NM_000251.3(MSH2):c.71A>G (p.Gln24Arg)]
NM_000251.3(MSH2):c.71A>G (p.Gln24Arg)
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
-
uncharacterized protein [Saccharomyces cerevisiae S288C]
uncharacterized protein [Saccharomyces cerevisiae S288C]Gene ID:850673Gene
-
Human DNA sequence from clone RP11-723P2 on chromosome X, complete sequence
Human DNA sequence from clone RP11-723P2 on chromosome X, complete sequencegi|22002718|emb|AL732326.4|Nucleotide
-
Taxonomy Links for Nucleotide (Select 1486587563) (1)
Taxonomy
-
Taxonomy Links for Protein (Select 189066554) (1)
Taxonomy
-
Taxonomy Links for Protein (Select 62897113) (1)
Taxonomy
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Dec 24, 2023