NM_000251.3(MSH2):c.2049G>A (p.Gly683=) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Sep 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001415353.15
Allele description [Variation Report for NM_000251.3(MSH2):c.2049G>A (p.Gly683=)]
NM_000251.3(MSH2):c.2049G>A (p.Gly683=)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
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7f84d12.x1 NCI_CGAP_Pr28 Homo sapiens cDNA clone IMAGE:3303671 3' similar to TR:...
7f84d12.x1 NCI_CGAP_Pr28 Homo sapiens cDNA clone IMAGE:3303671 3' similar to TR:O43633 O43633 BC-2 PROTEIN, mRNA sequencegi|10369527|gnl|dbEST|6184450|gb|BE 1.1|Nucleotide
-
603198972F1 NIH_MGC_96 Homo sapiens cDNA clone IMAGE:5278696 5', mRNA sequence
603198972F1 NIH_MGC_96 Homo sapiens cDNA clone IMAGE:5278696 5', mRNA sequencegi|15248634|gnl|dbEST|9252089|gb|BI 8.1|Nucleotide
-
nlk2 [Megalobrama amblycephala]
nlk2 [Megalobrama amblycephala]Gene ID:125249494Gene
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Last Updated: Oct 13, 2024