NM_000179.3(MSH6):c.4018_4032del (p.Ser1340_Thr1344del) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 9, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000629807.7
Allele description [Variation Report for NM_000179.3(MSH6):c.4018_4032del (p.Ser1340_Thr1344del)]
NM_000179.3(MSH6):c.4018_4032del (p.Ser1340_Thr1344del)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
Homo sapiens IGF like family member 2 (IGFL2), transcript variant 2, mRNA
Homo sapiens IGF like family member 2 (IGFL2), transcript variant 2, mRNAgi|1677531638|ref|NM_001135113.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024