NM_000455.5(STK11):c.863-7T>C AND Peutz-Jeghers syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001498337.14
Allele description [Variation Report for NM_000455.5(STK11):c.863-7T>C]
NM_000455.5(STK11):c.863-7T>C
Condition(s)
- Name:
- Peutz-Jeghers syndrome (PJS)
- Synonyms:
- POLYPOSIS, HAMARTOMATOUS INTESTINAL; POLYPS-AND-SPOTS SYNDROME; Peutz-Jeghers polyposis; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0008280; MeSH: D010580; MedGen: C0031269; Orphanet: 2869; OMIM: 175200
-
Homo sapiens regucalcin (senescence marker protein-30), mRNA (cDNA clone IMAGE:5...
Homo sapiens regucalcin (senescence marker protein-30), mRNA (cDNA clone IMAGE:5731957), partial cdsgi|37748317|gb|BC058880.1|Nucleotide
-
JGI_CABG7004.fwd NIH_XGC_tropSto1 Xenopus tropicalis cDNA clone CABG7004 5', mRN...
JGI_CABG7004.fwd NIH_XGC_tropSto1 Xenopus tropicalis cDNA clone CABG7004 5', mRNA sequencegi|71519312|gnl|dbEST|30382347|gb|D 24.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 20, 2024