NM_001382567.1(STIM1):c.1239-17C>G AND multiple conditions

This record was updated by the submitter. Please see the current version.

Germline classification:: Likely benign (1 submission)
Last evaluated:: Dec 4, 2022
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:: RCV002111362.7

Allele description

NM_001382567.1(STIM1):c.1239-17C>G

Gene:

STIM1:stromal interaction molecule 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.4

Genomic location:

Preferred name:

NM_001382567.1(STIM1):c.1239-17C>G

HGVS:

NC_000011.10:g.4083246C>G
NG_016277.1:g.232544C>G
NM_001277961.3:c.1239-17C>G
NM_001277962.2:c.1239-17C>G
NM_001382566.1:c.1017-17C>G
NM_001382567.1:c.1239-17C>GMANE SELECT
NM_001382568.1:c.1243C>G
NM_001382569.1:c.1104-17C>G
NM_001382570.1:c.1011-17C>G
NM_001382571.1:c.759-17C>G
NM_001382573.1:c.1017-17C>G
NM_001382575.1:c.1017-17C>G
NM_001382576.1:c.1017-17C>G
NM_001382577.1:c.1017-17C>G
NM_001382578.1:c.1017-17C>G
NM_001382579.1:c.1017-17C>G
NM_001382580.1:c.750-17C>G
NM_001382581.1:c.750-17C>G
NM_003156.4:c.1239-17C>G
NP_001369497.1:p.Leu415Val
LRG_164:g.232544C>G
NC_000011.9:g.4104476C>G

Protein change:

L415V

Links:

dbSNP: rs2094474498

NCBI 1000 Genomes Browser:

rs2094474498

Molecular consequence:

NM_001277961.3:c.1239-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001277962.2:c.1239-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382566.1:c.1017-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382567.1:c.1239-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382569.1:c.1104-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382570.1:c.1011-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382571.1:c.759-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382573.1:c.1017-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382575.1:c.1017-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382576.1:c.1017-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382577.1:c.1017-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382578.1:c.1017-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382579.1:c.1017-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382580.1:c.750-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382581.1:c.750-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_003156.4:c.1239-17C>G - intron variant - [Sequence Ontology: SO:0001627]
NM_001382568.1:c.1243C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Stormorken syndrome (STRMK)
Synonyms:: THROMBOCYTOPATHY, ASPLENIA, AND MIOSIS
Identifiers:: MONDO: MONDO:0008497; MedGen: C1861451; Orphanet: 3204; OMIM: 185070

Name:: Combined immunodeficiency due to STIM1 deficiency
Synonyms:: Immune dysfunction with T-cell inactivation due to calcium entry defect 2; STIM1 DEFICIENCY; IMMUNODEFICIENCY 10
Identifiers:: MONDO: MONDO:0013008; MedGen: C2748557; Orphanet: 169090; Orphanet: 317430; OMIM: 612783

Name:: Myopathy with tubular aggregates (TAM)
Synonyms:: Tubular Aggregate Myopathy
Identifiers:: MONDO: MONDO:0008051; MedGen: C0410207; OMIM: PS160565

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002385651	Invitae	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Likely benign (Dec 4, 2022)	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

SCV002385651

Invitae

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Likely benign
(Dec 4, 2022)

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	not provided	not provided	not provided	not provided	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

Details of each submission

From Invitae, SCV002385651.4

#	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

Last Updated: Mar 5, 2024

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