NM_000455.5(STK11):c.56C>T (p.Ser19Leu) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Dec 12, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000777388.7
Allele description [Variation Report for NM_000455.5(STK11):c.56C>T (p.Ser19Leu)]
NM_000455.5(STK11):c.56C>T (p.Ser19Leu)
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 thioredoxin domain containing 5 (TXNDC5), mRNA
Homo sapiens thioredoxin domain containing 5 (TXNDC5), mRNAgi|13540603|ref|NM_030810.1|Nucleotide
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BioAssay by Target (List) for Gene (Select 139378) (13)
PubChem BioAssay
-
coproporphyrinogen III oxidase [Pseudoalteromonas sp. XI10]
coproporphyrinogen III oxidase [Pseudoalteromonas sp. XI10]gi|966689745|gb|KTG22577.1||gnl|WGS |AUR67_00270Protein
-
calmodulin [Pseudoalteromonas sp. XI10]
calmodulin [Pseudoalteromonas sp. XI10]gi|966689733|gb|KTG22565.1||gnl|WGS |AUR67_00210Protein
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potassium transporter peripheral membrane component [Pseudoalteromonas sp. XI10]
potassium transporter peripheral membrane component [Pseudoalteromonas sp. XI10]gi|966689736|gb|KTG22568.1||gnl|WGS |AUR67_00225Protein
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See more...Assertion and evidence details
Last Updated: May 7, 2024