NM_000455.5(STK11):c.896C>A (p.Ser299Tyr) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 27, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002376239.2
Allele description [Variation Report for NM_000455.5(STK11):c.896C>A (p.Ser299Tyr)]
NM_000455.5(STK11):c.896C>A (p.Ser299Tyr)
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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See more...Assertion and evidence details
Last Updated: May 1, 2024