NM_020070.4(IGLL1):c.443C>T (p.Thr148Ile) AND not specified

Germline classification:: Benign (1 submission)
Last evaluated:: Jan 24, 2024
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:: RCV003490271.2

Allele description [Variation Report for NM_020070.4(IGLL1):c.443C>T (p.Thr148Ile)]

NM_020070.4(IGLL1):c.443C>T (p.Thr148Ile)

Gene:

IGLL1:immunoglobulin lambda like polypeptide 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

22q11.23

Genomic location:

Preferred name:

NM_020070.4(IGLL1):c.443C>T (p.Thr148Ile)

HGVS:

NC_000022.11:g.23573465G>A
NG_009791.1:g.11844C>T
NM_001369906.1:c.446C>T
NM_020070.4:c.443C>TMANE SELECT
NM_152855.3:c.*72C>T
NP_001356835.1:p.Thr149Ile
NP_064455.1:p.Thr148Ile
LRG_69:g.11844C>T
NC_000022.10:g.23915652G>A
NM_020070.3:c.443C>T

Protein change:

T148I

Links:

dbSNP: rs73157031

NCBI 1000 Genomes Browser:

rs73157031

Molecular consequence:

NM_152855.3:c.*72C>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
NM_001369906.1:c.446C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_020070.4:c.443C>T - missense variant - [Sequence Ontology: SO:0001583]

Observations:

Condition(s)

Synonyms:: AllHighlyPenetrant
Identifiers:: MedGen: CN169374

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004233494	Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Jan 24, 2024)	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

SCV004233494

Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Jan 24, 2024)

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	no	39	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

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 Unidad de Genómica Garrahan, Hospital de Pediatría Garrahan, SCV004233494.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	39	not provided	not provided	clinical testing	PubMed (1)

Description

This variant is classified as Benign based on local population frequency. This variant was detected in 41% of patients studied by a panel of primary immunodeficiencies. Number of patients: 39. Only high quality variants are reported.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	no	not provided	not provided	not provided		39	not provided	not provided	not provided

Last Updated: Sep 29, 2024

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