NM_001111.5(ADAR):c.2650G>A (p.Val884Ile) AND Inborn genetic diseases

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jun 21, 2023
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:: RCV003358015.2

Allele description [Variation Report for NM_001111.5(ADAR):c.2650G>A (p.Val884Ile)]

NM_001111.5(ADAR):c.2650G>A (p.Val884Ile)

Genes:

LOC126805874:CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:154561176-154562375 [Gene]
ADAR:adenosine deaminase RNA specific [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q21.3

Genomic location:

Preferred name:

NM_001111.5(ADAR):c.2650G>A (p.Val884Ile)

HGVS:

NC_000001.11:g.154589775C>T
NG_011844.2:g.46786G>A
NG_082198.1:g.1176C>T
NM_001025107.3:c.1765G>A
NM_001111.4:c.2650G>A
NM_001111.5:c.2650G>AMANE SELECT
NM_001193495.2:c.1765G>A
NM_001365045.1:c.2677G>A
NM_001365046.1:c.1765G>A
NM_001365047.1:c.1765G>A
NM_001365048.1:c.1765G>A
NM_001365049.1:c.1687G>A
NM_015840.4:c.2572G>A
NM_015841.4:c.2515G>A
NP_001020278.1:p.Val589Ile
NP_001102.3:p.Val884Ile
NP_001180424.1:p.Val589Ile
NP_001351974.1:p.Val893Ile
NP_001351975.1:p.Val589Ile
NP_001351976.1:p.Val589Ile
NP_001351977.1:p.Val589Ile
NP_001351978.1:p.Val563Ile
NP_056655.3:p.Val858Ile
NP_056656.3:p.Val839Ile
LRG_1212t1:c.2650G>A
LRG_1212:g.46786G>A
LRG_1212p1:p.Val884Ile
NC_000001.10:g.154562251C>T

Protein change:

V563I

Molecular consequence:

NM_001025107.3:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001111.5:c.2650G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001193495.2:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001365045.1:c.2677G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001365046.1:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001365047.1:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001365048.1:c.1765G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001365049.1:c.1687G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_015840.4:c.2572G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_015841.4:c.2515G>A - 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
SCV004076665	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Uncertain significance (Jun 21, 2023)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004076665

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Uncertain significance
(Jun 21, 2023)

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, SCV004076665.2

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

Description

The c.2650G>A (p.V884I) alteration is located in exon 8 (coding exon 8) of the ADAR gene. This alteration results from a G to A substitution at nucleotide position 2650, causing the valine (V) at amino acid position 884 to be replaced by an isoleucine (I). 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: Sep 29, 2024

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