NM_000251.3(MSH2):c.2162G>C (p.Gly721Ala) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 2, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003758458.1
Allele description [Variation Report for NM_000251.3(MSH2):c.2162G>C (p.Gly721Ala)]
NM_000251.3(MSH2):c.2162G>C (p.Gly721Ala)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
cAMP-responsive element modulator isoform 19 [Homo sapiens]
cAMP-responsive element modulator isoform 19 [Homo sapiens]gi|34335226|ref|NP_898831.1|Protein
-
Sptbn5 spectrin beta, non-erythrocytic 5 [Mus musculus]
Sptbn5 spectrin beta, non-erythrocytic 5 [Mus musculus]Gene ID:640524Gene
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Last Updated: Feb 28, 2024