NM_003331.5(TYK2):c.844C>G (p.Leu282Val) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: May 11, 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:: RCV002846039.2

Allele description [Variation Report for NM_003331.5(TYK2):c.844C>G (p.Leu282Val)]

NM_003331.5(TYK2):c.844C>G (p.Leu282Val)

Gene:

TYK2:tyrosine kinase 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.2

Genomic location:

Preferred name:

NM_003331.5(TYK2):c.844C>G (p.Leu282Val)

HGVS:

NC_000019.10:g.10365684G>C
NG_007872.1:g.19889C>G
NM_001385197.1:c.844C>G
NM_001385198.1:c.844C>G
NM_001385199.1:c.844C>G
NM_001385200.1:c.844C>G
NM_001385201.1:c.844C>G
NM_001385202.1:c.844C>G
NM_001385203.1:c.844C>G
NM_001385204.1:c.844C>G
NM_001385205.1:c.754C>G
NM_001385206.1:c.844C>G
NM_001385207.1:c.844C>G
NM_001406461.1:c.844C>G
NM_003331.5:c.844C>GMANE SELECT
NP_001372126.1:p.Leu282Val
NP_001372127.1:p.Leu282Val
NP_001372128.1:p.Leu282Val
NP_001372129.1:p.Leu282Val
NP_001372130.1:p.Leu282Val
NP_001372131.1:p.Leu282Val
NP_001372132.1:p.Leu282Val
NP_001372133.1:p.Leu282Val
NP_001372134.1:p.Leu252Val
NP_001372135.1:p.Leu282Val
NP_001372136.1:p.Leu282Val
NP_001393390.1:p.Leu282Val
NP_003322.3:p.Leu282Val
NP_003322.3:p.Leu282Val
LRG_121t1:c.844C>G
LRG_121:g.19889C>G
LRG_121p1:p.Leu282Val
NC_000019.9:g.10476360G>C
NM_003331.4:c.844C>G

Protein change:

L252V

Molecular consequence:

NM_001385197.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385198.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385199.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385200.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385201.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385202.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385203.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385204.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385205.1:c.754C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385206.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001385207.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_001406461.1:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]
NM_003331.5:c.844C>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Inborn genetic diseases
Identifiers:: MeSH: D030342; MedGen: C0950123

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV003617231	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (May 11, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003617231

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(May 11, 2022)

germline

clinical testing

Citation Link

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

Details of each submission

From Ambry Genetics, SCV003617231.2

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

Description

The c.844C>G (p.L282V) alteration is located in exon 7 (coding exon 5) of the TYK2 gene. This alteration results from a C to G substitution at nucleotide position 844, causing the leucine (L) at amino acid position 282 to be replaced by a valine (V). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

#	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: May 1, 2024

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