NM_000251.3(MSH2):c.335C>T (p.Ser112Phe) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001211169.6
Allele description [Variation Report for NM_000251.3(MSH2):c.335C>T (p.Ser112Phe)]
NM_000251.3(MSH2):c.335C>T (p.Ser112Phe)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Homo sapiens sorting nexin 8 (SNX8), mRNA
Homo sapiens sorting nexin 8 (SNX8), mRNAgi|1519242511|ref|NM_013321.4|Nucleotide
-
LOC102065237 [Zonotrichia albicollis]
LOC102065237 [Zonotrichia albicollis]Gene ID:102065237Gene
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Last Updated: Sep 29, 2024