NM_005751.5(AKAP9):c.8375A>G (p.Asn2792Ser) AND Congenital long QT syndrome

Germline classification:: Likely benign (1 submission)
Last evaluated:: Jun 14, 2016
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:: RCV000261848.5

Allele description [Variation Report for NM_005751.5(AKAP9):c.8375A>G (p.Asn2792Ser)]

NM_005751.5(AKAP9):c.8375A>G (p.Asn2792Ser)

Gene:

AKAP9:A-kinase anchoring protein 9 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

7q21.2

Genomic location:

Preferred name:

NM_005751.5(AKAP9):c.8375A>G (p.Asn2792Ser)

Other names:

p.N2792S:AAT>AGT

HGVS:

NC_000007.14:g.92083384A>G
NG_011623.1:g.147510A>G
NM_001379277.1:c.3020A>G
NM_005751.5:c.8375A>GMANE SELECT
NM_147185.3:c.8351A>G
NP_001366206.1:p.Asn1007Ser
NP_005742.4:p.Asn2792Ser
NP_005742.4:p.Asn2792Ser
NP_671714.1:p.Asn2784Ser
LRG_331t1:c.8375A>G
LRG_331:g.147510A>G
LRG_331p1:p.Asn2792Ser
NC_000007.13:g.91712698A>G
NM_005751.4:c.8375A>G

Protein change:

N1007S

Links:

dbSNP: rs6960867

NCBI 1000 Genomes Browser:

rs6960867

Molecular consequence:

NM_001379277.1:c.3020A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_005751.5:c.8375A>G - missense variant - [Sequence Ontology: SO:0001583]
NM_147185.3:c.8351A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Congenital long QT syndrome (RWS)
Synonyms:: Familial long QT syndrome; Romano-Ward syndrome; Ventricular fibrillation with prolonged QT interval
Identifiers:: MONDO: MONDO:0019171; MedGen: C1141890; Orphanet: 768; OMIM: PS192500

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000470305	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification 20161018)	Likely benign (Jun 14, 2016)	germline	clinical testing	ICSL_Variant_Classification_20161018.pdf Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000470305

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification 20161018)

Likely benign
(Jun 14, 2016)

germline

clinical testing

ICSL_Variant_Classification_20161018.pdf

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 Illumina Laboratory Services, Illumina, SCV000470305.2

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

#	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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