NM_000251.3(MSH2):c.1809T>C (p.Asp603=) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 6, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001013262.3
Allele description [Variation Report for NM_000251.3(MSH2):c.1809T>C (p.Asp603=)]
NM_000251.3(MSH2):c.1809T>C (p.Asp603=)
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
-
LOC115148613 [Salmo trutta]
LOC115148613 [Salmo trutta]Gene ID:115148613Gene
-
EYB26_003946 [Talaromyces marneffei]
EYB26_003946 [Talaromyces marneffei]Gene ID:79163919Gene
-
A1Q1_06847 [Trichosporon asahii var. asahii CBS 2479]
A1Q1_06847 [Trichosporon asahii var. asahii CBS 2479]Gene ID:25990359Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024