NM_000455.5(STK11):c.1109-15C>T AND Peutz-Jeghers syndrome

Germline classification:: Likely benign (2 submissions)
Last evaluated:: Apr 3, 2023
Review status:: 2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts

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:: RCV003617850.4

Allele description [Variation Report for NM_000455.5(STK11):c.1109-15C>T]

NM_000455.5(STK11):c.1109-15C>T

Gene:

STK11:serine/threonine kinase 11 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.3

Genomic location:

Preferred name:

NM_000455.5(STK11):c.1109-15C>T

HGVS:

NC_000019.10:g.1226439C>T
NG_007460.2:g.42033C>T
NM_000455.5:c.1109-15C>TMANE SELECT
LRG_319t1:c.1109-15C>T
LRG_319:g.42033C>T
NC_000019.9:g.1226438C>T
NM_000455.4:c.1109-15C>T

Links:

dbSNP: rs1057520799

NCBI 1000 Genomes Browser:

rs1057520799

Molecular consequence:

NM_000455.5:c.1109-15C>T - intron variant - [Sequence Ontology: SO:0001627]

Observations:

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

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PREDICTED: Glycine max dof zinc finger protein DOF3.1 (LOC778096), mRNA
PREDICTED: Glycine max dof zinc finger protein DOF3.1 (LOC778096), mRNA
gi|2027505824|ref|XM_003543559.5|

Nucleotide
PREDICTED: Mus musculus ARP1 actin-related protein 1B, centractin beta (Actr1b),...
PREDICTED: Mus musculus ARP1 actin-related protein 1B, centractin beta (Actr1b), transcript variant X3, mRNA
gi|1907068531|ref|XM_036164312.1|

Nucleotide
Odontocolon mellipes voucher BF001217 28S ribosomal RNA gene, partial sequence
Odontocolon mellipes voucher BF001217 28S ribosomal RNA gene, partial sequence
gi|183988410|gb|EU378903.1|

Nucleotide
BX710390 XGC-tadpole Xenopus tropicalis cDNA clone TTpA003f10 3', mRNA sequence
BX710390 XGC-tadpole Xenopus tropicalis cDNA clone TTpA003f10 3', mRNA sequence
gi|38382493|gnl|dbEST|20427524|emb| 390.1|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004534055	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Mar 26, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]
SCV004824233	All of Us Research Program, National Institutes of Health	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely Benign (Apr 3, 2023)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004534055

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Mar 26, 2023)

germline

clinical testing

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

SCV004824233

All of Us Research Program, National Institutes of Health

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely Benign
(Apr 3, 2023)

germline

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	1	not provided	not provided	108544	not provided	clinical 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

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]

PMID:: 25741868
PMCID:: PMC4544753

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV004534055.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

From All of Us Research Program, National Institutes of Health, SCV004824233.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	1	not provided	not provided	clinical testing	PubMed (1)

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	108544	not provided	not provided		1	not provided	not provided	not provided

Last Updated: Oct 8, 2024

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