NM_000251.3(MSH2):c.2042A>T (p.Gln681Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002419954.2
Allele description [Variation Report for NM_000251.3(MSH2):c.2042A>T (p.Gln681Leu)]
NM_000251.3(MSH2):c.2042A>T (p.Gln681Leu)
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
-
ACSF3 [Desmodus rotundus]
ACSF3 [Desmodus rotundus]Gene ID:112300687Gene
-
LOC110508309 [Oncorhynchus mykiss]
LOC110508309 [Oncorhynchus mykiss]Gene ID:110508309Gene
-
AFUA_4G03000 [Aspergillus fumigatus Af293]
AFUA_4G03000 [Aspergillus fumigatus Af293]Gene ID:3503855Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024