rs4752307

Variant names:

• chr10-119422897-G-A
• rs4752307
• NM_005308.3:c.340-269G>A

Your query was ambiguous. Multiple possible variants found:

• chr10-119422897-G-A
• chr10-119422897-G-C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_005308.3(GRK5):​c.340-269G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.372 in 152,160 control chromosomes in the GnomAD database, including 12,056 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.37 (12056 hom., cov: 33)
• Consequence: GRK5 NM_005308.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.07
• Publications: 3 publications found

Genes affected

GRK5 (HGNC:4544): (G protein-coupled receptor kinase 5) This gene encodes a member of the guanine nucleotide-binding protein (G protein)-coupled receptor kinase subfamily of the Ser/Thr protein kinase family. The protein phosphorylates the activated forms of G protein-coupled receptors thus initiating their deactivation. It has also been shown to play a role in regulating the motility of polymorphonuclear leukocytes (PMNs). [provided by RefSeq, Jul 2008]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.572 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GRK5	NM_005308.3	c.340-269G>A		intron_variant	Intron 4 of 15	ENST00000392870.3	NP_005299.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GRK5	ENST00000392870.3	c.340-269G>A		intron_variant	Intron 4 of 15	1	NM_005308.3	ENSP00000376609.2

Frequencies

GnomAD3 genomes AF: 0.372 AC: 56528 AN: 152042 Hom.: 12018 Cov.: 33

Gnomad AFR AF: 0.577

Gnomad AMI AF: 0.257

Gnomad AMR AF: 0.287

Gnomad ASJ AF: 0.191

Gnomad EAS AF: 0.557

Gnomad SAS AF: 0.337

Gnomad FIN AF: 0.341

Gnomad MID AF: 0.206

Gnomad NFE AF: 0.272

Gnomad OTH AF: 0.346

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.372 AC: 56624 AN: 152160 Hom.: 12056 Cov.: 33 AF XY: 0.373 AC XY: 27764 AN XY: 74370

African (AFR) AF: 0.578 AC: 23976 AN: 41506

American (AMR) AF: 0.287 AC: 4391 AN: 15300

Ashkenazi Jewish (ASJ) AF: 0.191 AC: 662 AN: 3468

East Asian (EAS) AF: 0.557 AC: 2882 AN: 5172

South Asian (SAS) AF: 0.336 AC: 1619 AN: 4824

European-Finnish (FIN) AF: 0.341 AC: 3606 AN: 10580

Middle Eastern (MID) AF: 0.190 AC: 56 AN: 294

European-Non Finnish (NFE) AF: 0.272 AC: 18461 AN: 67994

Other (OTH) AF: 0.349 AC: 738 AN: 2114

Alfa AF: 0.346 Hom.: 1966

Bravo AF: 0.379

Asia WGS AF: 0.490 AC: 1701 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.079
DANN	Benign	0.57
PhyloP100		-2.1
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

Other links and lift over

dbSNP: rs4752307; hg19: chr10-121182409;