U.S. flag

An official website of the United States government

NM_000455.5(STK11):c.1197_1198delinsAT (p.Gln399_Leu400=) AND Peutz-Jeghers syndrome

Germline classification:
Likely benign (1 submission)
Last evaluated:
Jan 14, 2019
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000981453.9

Allele description [Variation Report for NM_000455.5(STK11):c.1197_1198delinsAT (p.Gln399_Leu400=)]

NM_000455.5(STK11):c.1197_1198delinsAT (p.Gln399_Leu400=)

Gene:
STK11:serine/threonine kinase 11 [Gene - OMIM - HGNC]
Variant type:
Indel
Cytogenetic location:
19p13.3
Genomic location:
Preferred name:
NM_000455.5(STK11):c.1197_1198delinsAT (p.Gln399_Leu400=)
HGVS:
  • NC_000019.10:g.1226542_1226543delinsAT
  • NG_007460.2:g.42136_42137delinsAT
  • NM_000455.5:c.1197_1198delinsATMANE SELECT
  • NP_000446.1:p.Gln399_Leu400=
  • NP_000446.1:p.Gln399_Leu400=
  • LRG_319t1:c.1197_1198delinsAT
  • LRG_319:g.42136_42137delinsAT
  • NC_000019.9:g.1226541_1226542delinsAT
  • NM_000455.4:c.1197_1198delGCinsAT
  • NM_000455.4:c.1197_1198delinsAT
  • NR_176325.1:n.2464_2465delinsAT
Links:
dbSNP: rs1599932274
NCBI 1000 Genomes Browser:
rs1599932274
Molecular consequence:
  • NR_176325.1:n.2464_2465delinsAT - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NM_000455.5:c.1197_1198delinsAT - synonymous variant - [Sequence Ontology: SO:0001819]

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

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001129426Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Likely benign
(Jan 14, 2019) 		germlineclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group., Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]
PMID:
28492532
PMCID:
PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001129426.6

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Oct 8, 2024