NM_000249.4(MLH1):c.2086A>G (p.Thr696Ala) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 3, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002423172.2
Allele description [Variation Report for NM_000249.4(MLH1):c.2086A>G (p.Thr696Ala)]
NM_000249.4(MLH1):c.2086A>G (p.Thr696Ala)
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
Homo sapiens HMT1 hnRNP methyltransferase-like 3 (S. cerevisiae) (HRMT1L3), mRNA
Homo sapiens HMT1 hnRNP methyltransferase-like 3 (S. cerevisiae) (HRMT1L3), mRNAgi|9789978|ref|NM_019854.1|Nucleotide
-
DC170940 Xenopus tropicalis embryo gastrula Xenopus tropicalis cDNA clone st27h1...
DC170940 Xenopus tropicalis embryo gastrula Xenopus tropicalis cDNA clone st27h15 5', mRNA sequencegi|119149897|gnl|dbEST|43414682|dbj 0940.1|Nucleotide
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Last Updated: Sep 29, 2024