NM_000179.3(MSH6):c.988T>C (p.Ser330Pro) AND Hereditary nonpolyposis colorectal neoplasms
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001055886.8
Allele description [Variation Report for NM_000179.3(MSH6):c.988T>C (p.Ser330Pro)]
NM_000179.3(MSH6):c.988T>C (p.Ser330Pro)
Condition(s)
- Name:
- Hereditary nonpolyposis colorectal neoplasms
- Identifiers:
- MeSH: D003123; MedGen: C0009405
-
very long chain fatty acid elongase 5 isoform 2 [Homo sapiens]
very long chain fatty acid elongase 5 isoform 2 [Homo sapiens]gi|338827646|ref|NP_001229757.1|Protein
-
CNBI3410 [Cryptococcus neoformans var. neoformans B-3501A]
CNBI3410 [Cryptococcus neoformans var. neoformans B-3501A]Gene ID:4938303Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024