NM_000179.3(MSH6):c.3500T>A (p.Leu1167His) AND Lynch syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004004604.2
Allele description [Variation Report for NM_000179.3(MSH6):c.3500T>A (p.Leu1167His)]
NM_000179.3(MSH6):c.3500T>A (p.Leu1167His)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
Homo sapiens zinc finger protein 672, mRNA (cDNA clone IMAGE:5175166)
Homo sapiens zinc finger protein 672, mRNA (cDNA clone IMAGE:5175166)gi|20381058|gb|BC029310.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024