NM_000179.3(MSH6):c.2699G>A (p.Gly900Asp) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001893047.3
Allele description [Variation Report for NM_000179.3(MSH6):c.2699G>A (p.Gly900Asp)]
NM_000179.3(MSH6):c.2699G>A (p.Gly900Asp)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Homo sapiens nuclear receptor subfamily 4 group A member 3 (NR4A3), transcript v...
Homo sapiens nuclear receptor subfamily 4 group A member 3 (NR4A3), transcript variant 3, mRNAgi|1890259025|ref|NM_173200.3|Nucleotide
-
Crenarchaeote SCGC AAA288-P02 small subunit ribosomal RNA gene, partial sequence
Crenarchaeote SCGC AAA288-P02 small subunit ribosomal RNA gene, partial sequencegi|322512529|gb|HQ675854.1|Nucleotide
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Last Updated: Feb 20, 2024