NM_000179.3(MSH6):c.3963A>G (p.Arg1321=) AND Lynch syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 1, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000758627.3
Allele description [Variation Report for NM_000179.3(MSH6):c.3963A>G (p.Arg1321=)]
NM_000179.3(MSH6):c.3963A>G (p.Arg1321=)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
secretory carrier-associated membrane protein 4 isoform 3 [Homo sapiens]
secretory carrier-associated membrane protein 4 isoform 3 [Homo sapiens]gi|1043915977|ref|NP_001316469.1|Protein
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Last Updated: Dec 24, 2023