NM_000251.3(MSH2):c.178A>C (p.Thr60Pro) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 23, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001965976.3
Allele description [Variation Report for NM_000251.3(MSH2):c.178A>C (p.Thr60Pro)]
NM_000251.3(MSH2):c.178A>C (p.Thr60Pro)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Homo sapiens gap junction protein, alpha 5, 40kD (connexin 40) (GJA5), mRNA
Homo sapiens gap junction protein, alpha 5, 40kD (connexin 40) (GJA5), mRNAgi|6631082|ref|NM_005266.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Feb 20, 2024