NM_006564.2(CXCR6):c.847C>T (p.Leu283Phe) AND not specified

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 27, 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:: RCV004166590.1

Allele description [Variation Report for NM_006564.2(CXCR6):c.847C>T (p.Leu283Phe)]

NM_006564.2(CXCR6):c.847C>T (p.Leu283Phe)

Genes:

CXCR6:C-X-C motif chemokine receptor 6 [Gene - OMIM - HGNC]
FYCO1:FYVE and coiled-coil domain autophagy adaptor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p21.31

Genomic location:

Preferred name:

NM_006564.2(CXCR6):c.847C>T (p.Leu283Phe)

HGVS:

NC_000003.12:g.45947328C>T
NG_031955.1:g.53497G>A
NM_001386421.1:c.3944+7921G>A
NM_001386422.1:c.3944+7921G>A
NM_001386423.1:c.3941+7921G>A
NM_001386424.1:c.3944+7921G>A
NM_001386425.1:c.3944+7921G>A
NM_001386426.1:c.3824+7921G>A
NM_001386427.1:c.3800+7921G>A
NM_001386428.1:c.3944+7921G>A
NM_001386429.1:c.3944+7921G>A
NM_001386430.1:c.3344+7921G>A
NM_001386435.1:c.847C>T
NM_001386436.1:c.847C>T
NM_001386437.1:c.847C>T
NM_006564.2:c.847C>TMANE SELECT
NM_024513.4:c.3944+7921G>AMANE SELECT
NP_001373364.1:p.Leu283Phe
NP_001373365.1:p.Leu283Phe
NP_001373366.1:p.Leu283Phe
NP_006555.1:p.Leu283Phe
NC_000003.11:g.45988820C>T
NM_006564.1:c.847C>T

Protein change:

L283F

Molecular consequence:

NM_001386421.1:c.3944+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001386422.1:c.3944+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001386423.1:c.3941+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001386424.1:c.3944+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001386425.1:c.3944+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001386426.1:c.3824+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001386427.1:c.3800+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001386428.1:c.3944+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001386429.1:c.3944+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001386430.1:c.3344+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_024513.4:c.3944+7921G>A - intron variant - [Sequence Ontology: SO:0001627]
NM_001386435.1:c.847C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001386436.1:c.847C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001386437.1:c.847C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_006564.2:c.847C>T - missense variant - [Sequence Ontology: SO:0001583]

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
SCV003647797	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Oct 27, 2022)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV003647797

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Oct 27, 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, SCV003647797.2

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

Description

The c.847C>T (p.L283F) alteration is located in exon 2 (coding exon 1) of the CXCR6 gene. This alteration results from a C to T substitution at nucleotide position 847, causing the leucine (L) at amino acid position 283 to be replaced by a phenylalanine (F). 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: Nov 24, 2024

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