rs7176605

chr15-85443491-G-Achr15-85443491-G-C

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_007200.5(AKAP13):c.-11-42219G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.77 in 152,014 control chromosomes in the GnomAD database, including 45,439 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 0.77 (45439 hom., cov: 31)
• Consequence: AKAP13 NM_007200.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.66

Genes affected

AKAP13 (HGNC:371): (A-kinase anchoring protein 13) The A-kinase anchor proteins (AKAPs) are a group of structurally diverse proteins which have the common function of binding to the regulatory subunit of protein kinase A (PKA) and confining the holoenzyme to discrete locations within the cell. This gene encodes a member of the AKAP family. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms containing c-terminal dbl oncogene homology (DH) and pleckstrin homology (PH) domains. The DH domain is associated with guanine nucleotide exchange activation for the Rho/Rac family of small GTP binding proteins, resulting in the conversion of the inactive GTPase to the active form capable of transducing signals. The PH domain has multiple functions. Therefore, these isoforms function as scaffolding proteins to coordinate a Rho signaling pathway, function as protein kinase A-anchoring proteins and, in addition, enhance ligand-dependent activity of estrogen receptors alpha and beta. [provided by RefSeq, Jul 2012]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.798 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
AKAP13	NM_007200.5	c.-11-42219G>A		intron_variant		ENST00000394518.7
AKAP13	NM_006738.6	c.-11-42219G>A		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
AKAP13	ENST00000394518.7	c.-11-42219G>A		intron_variant		1	NM_007200.5	A2

Frequencies

GnomAD3 genomes AF: 0.770 AC: 116981 AN: 151896 Hom.: 45419 Cov.: 31

Gnomad AFR AF: 0.806

Gnomad AMI AF: 0.857

Gnomad AMR AF: 0.746

Gnomad ASJ AF: 0.761

Gnomad EAS AF: 0.526

Gnomad SAS AF: 0.604

Gnomad FIN AF: 0.710

Gnomad MID AF: 0.750

Gnomad NFE AF: 0.793

Gnomad OTH AF: 0.759

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

GnomAD4 genome AF: 0.770 AC: 117059 AN: 152014 Hom.: 45439 Cov.: 31 AF XY: 0.761 AC XY: 56549 AN XY: 74320

Gnomad4 AFR AF: 0.806

Gnomad4 AMR AF: 0.746

Gnomad4 ASJ AF: 0.761

Gnomad4 EAS AF: 0.526

Gnomad4 SAS AF: 0.604

Gnomad4 FIN AF: 0.710

Gnomad4 NFE AF: 0.793

Gnomad4 OTH AF: 0.754

Alfa AF: 0.778 Hom.: 5425

Bravo AF: 0.781

Asia WGS AF: 0.564 AC: 1958 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
Cadd	Benign	0.034
Dann	Benign	0.78

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

LitVar

Other links and lift over

dbSNP: rs7176605; hg19: chr15-85986722;