NM_000179.3(MSH6):c.3713C>G (p.Thr1238Ser) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 26, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000458549.8
Allele description [Variation Report for NM_000179.3(MSH6):c.3713C>G (p.Thr1238Ser)]
NM_000179.3(MSH6):c.3713C>G (p.Thr1238Ser)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
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Sample from Halorubrum hochstenium ATCC 700873
Sample from Halorubrum hochstenium ATCC 700873biosample
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BioSample links for Nucleotide (Select 448539122) (1)
BioSample
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BioSample links for Nucleotide (Select 448537265) (0)
BioSample
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024