NM_000251.3(MSH2):c.2083G>C (p.Val695Leu) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001226997.8
Allele description [Variation Report for NM_000251.3(MSH2):c.2083G>C (p.Val695Leu)]
NM_000251.3(MSH2):c.2083G>C (p.Val695Leu)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Riboflavin biosynthesis protein ribF (Includes: Riboflavin kinase; FMN adenylylt...
Riboflavin biosynthesis protein ribF (Includes: Riboflavin kinase; FMN adenylyltransferase) [Nostocoides jenkinsii Ben 74]gi|665500461|emb|CCI51596.1|Protein
-
hypothetical protein BN13_1090030 [Nostocoides jenkinsii Ben 74]
hypothetical protein BN13_1090030 [Nostocoides jenkinsii Ben 74]gi|665500460|emb|CCI51595.1|Protein
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Last Updated: Sep 29, 2024