NM_000251.3(MSH2):c.441del (p.Val148fs) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Dec 23, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003094691.2
Allele description
NM_000251.3(MSH2):c.441del (p.Val148fs)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Homo sapiens full length insert cDNA clone YB31A06
Homo sapiens full length insert cDNA clone YB31A06gi|4761693|gb|AF147342.1|AF147342Nucleotide
-
Homo sapiens ankyrin repeat domain 13D (ANKRD13D), transcript variant 1, mRNA
Homo sapiens ankyrin repeat domain 13D (ANKRD13D), transcript variant 1, mRNAgi|1696048206|ref|NM_207354.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024