NM_000251.3(MSH2):c.1841G>C (p.Gly614Ala) AND Lynch syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004013590.2
Allele description [Variation Report for NM_000251.3(MSH2):c.1841G>C (p.Gly614Ala)]
NM_000251.3(MSH2):c.1841G>C (p.Gly614Ala)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
Mus musculus LYR motif containing 7, mRNA (cDNA clone MGC:171033 IMAGE:8862428),...
Mus musculus LYR motif containing 7, mRNA (cDNA clone MGC:171033 IMAGE:8862428), complete cdsgi|187951434|gb|BC139406.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024