chr9-77728671-G-GA

Variant names:

• chr9-77728671-G-GA
• rs5898555
• NM_002072.5:c.736-5dupT

Variant summary

Our verdict is Benign. The variant received -16 ACMG points: 0P and 16B. BP6_Very_Strong BA1

The NM_002072.5(GNAQ):​c.736-5dupT variant causes a splice region, intron change involving the alteration of a non-conserved nucleotide. 1/1 splice prediction tools predict no significant impact on normal splicing. Variant has been reported in ClinVar as Benign (★★).

• Frequency:
  • Genomes: 𝑓 0.62 (28650 hom., cov: 0)
  • Exomes 𝑓: 0.46 (11433 hom.)
  • Failed GnomAD Quality Control
• Consequence: GNAQ NM_002072.5 splice_region, intron
• Clinical Significance: Benign criteria provided, multiple submitters, no conflicts B:5
• Conservation: PhyloP100: -0.572

Genes affected

GNAQ (HGNC:4390): (G protein subunit alpha q) This locus encodes a guanine nucleotide-binding protein. The encoded protein, an alpha subunit in the Gq class, couples a seven-transmembrane domain receptor to activation of phospolipase C-beta. Mutations at this locus have been associated with problems in platelet activation and aggregation. A related pseudogene exists on chromosome 2.[provided by RefSeq, Nov 2010]

ACMG classification

Our verdict: Benign. The variant received -16 ACMG points.

• BP6: Variant 9-77728671-G-GA is Benign according to our data. Variant chr9-77728671-G-GA is described in ClinVar as [Benign]. Clinvar id is 768309.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.698 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GNAQ	NM_002072.5	c.736-5dupT		splice_region_variant, intron_variant	Intron 5 of 6	ENST00000286548.9	NP_002063.2
GNAQ	XM_047423239.1	c.562-5dupT		splice_region_variant, intron_variant	Intron 5 of 6		XP_047279195.1
GNAQ	XM_047423240.1	c.562-5dupT		splice_region_variant, intron_variant	Intron 5 of 6		XP_047279196.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GNAQ	ENST00000286548.9	c.736-5_736-4insT		splice_region_variant, intron_variant	Intron 5 of 6	1	NM_002072.5	ENSP00000286548.4

Frequencies

GnomAD3 genomes AF: 0.624 AC: 90799 AN: 145520 Hom.: 28662 Cov.: 0

Gnomad AFR AF: 0.483

Gnomad AMI AF: 0.745

Gnomad AMR AF: 0.679

Gnomad ASJ AF: 0.666

Gnomad EAS AF: 0.440

Gnomad SAS AF: 0.604

Gnomad FIN AF: 0.642

Gnomad MID AF: 0.702

Gnomad NFE AF: 0.703

Gnomad OTH AF: 0.638

GnomAD2 exomes AF: 0.461 AC: 78870 AN: 170990 AF XY: 0.464

Gnomad AFR exome AF: 0.405

Gnomad AMR exome AF: 0.464

Gnomad ASJ exome AF: 0.466

Gnomad EAS exome AF: 0.405

Gnomad FIN exome AF: 0.466

Gnomad NFE exome AF: 0.477

Gnomad OTH exome AF: 0.466

GnomAD4 exome Data not reliable, filtered out with message: InbreedingCoeff AF: 0.456 AC: 531446 AN: 1165842 Hom.: 11433 Cov.: 22 AF XY: 0.455 AC XY: 266289 AN XY: 584788

African (AFR) AF: 0.372 AC: 9789 AN: 26302

American (AMR) AF: 0.445 AC: 12853 AN: 28900

Ashkenazi Jewish (ASJ) AF: 0.448 AC: 9390 AN: 20942

East Asian (EAS) AF: 0.387 AC: 13720 AN: 35438

South Asian (SAS) AF: 0.433 AC: 29880 AN: 69022

European-Finnish (FIN) AF: 0.445 AC: 18805 AN: 42228

Middle Eastern (MID) AF: 0.463 AC: 2095 AN: 4522

European-Non Finnish (NFE) AF: 0.464 AC: 412844 AN: 889340

Other (OTH) AF: 0.449 AC: 22070 AN: 49148

GnomAD4 genome AF: 0.624 AC: 90796 AN: 145586 Hom.: 28650 Cov.: 0 AF XY: 0.619 AC XY: 43713 AN XY: 70562

African (AFR) AF: 0.483 AC: 19107 AN: 39580

American (AMR) AF: 0.679 AC: 9960 AN: 14678

Ashkenazi Jewish (ASJ) AF: 0.666 AC: 2280 AN: 3422

East Asian (EAS) AF: 0.439 AC: 2163 AN: 4922

South Asian (SAS) AF: 0.604 AC: 2781 AN: 4602

European-Finnish (FIN) AF: 0.642 AC: 5599 AN: 8722

Middle Eastern (MID) AF: 0.688 AC: 190 AN: 276

European-Non Finnish (NFE) AF: 0.703 AC: 46760 AN: 66468

Other (OTH) AF: 0.637 AC: 1281 AN: 2010

Alfa AF: 0.00 Hom.: 0

ClinVar

Significance: Benign

Submissions summary: Benign:5

Revision: criteria provided, multiple submitters, no conflicts

Submissions by phenotype

not provided Benign:3

May 04, 2021

GeneDx

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

-

Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC)

Significance: Likely benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

- -

Dec 31, 2019

Labcorp Genetics (formerly Invitae), Labcorp

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

not specified Benign:2

Feb 16, 2025

Laboratory of Genetics, Children's Clinical University Hospital Latvia

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

-

Clinical Genetics, Academic Medical Center

Significance: Benign

Review Status: no assertion criteria provided

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
PhyloP100		-0.57
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

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Other links and lift over

dbSNP: rs5898555; hg19: chr9-80343587;