NM_000179.3(MSH6):c.1192G>C (p.Val398Leu) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000706608.7
Allele description [Variation Report for NM_000179.3(MSH6):c.1192G>C (p.Val398Leu)]
NM_000179.3(MSH6):c.1192G>C (p.Val398Leu)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Rattus norvegicus p55 protein, mRNA (cDNA clone MGC:108959 IMAGE:7127032), compl...
Rattus norvegicus p55 protein, mRNA (cDNA clone MGC:108959 IMAGE:7127032), complete cdsgi|60552124|gb|BC091223.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024