NM_000251.3(MSH2):c.1831G>A (p.Val611Met) AND Lynch syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 30, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003998756.2
Allele description [Variation Report for NM_000251.3(MSH2):c.1831G>A (p.Val611Met)]
NM_000251.3(MSH2):c.1831G>A (p.Val611Met)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
host cell factor isoform X1 [Eupeodes corollae]
host cell factor isoform X1 [Eupeodes corollae]gi|2503835251|ref|XP_055922520.1|Protein
-
yl61h06.s1 Soares breast 3NbHBst Homo sapiens cDNA clone IMAGE:162779 3', mRNA s...
yl61h06.s1 Soares breast 3NbHBst Homo sapiens cDNA clone IMAGE:162779 3', mRNA sequencegi|897555|gnl|dbEST|288112|gb|H2756Nucleotide
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Last Updated: Jun 9, 2024