rs10131032

chr14-32780875-G-A

Variant summary

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

The NM_004274.5(AKAP6):c.3588+6982G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0953 in 152,044 control chromosomes in the GnomAD database, including 746 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 0.095 (746 hom., cov: 32)
• Consequence: AKAP6 NM_004274.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.00300

Genes affected

AKAP6 (HGNC:376): (A-kinase anchoring protein 6) 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. The encoded protein is highly expressed in various brain regions and cardiac and skeletal muscle. It is specifically localized to the sarcoplasmic reticulum and nuclear membrane, and is involved in anchoring PKA to the nuclear membrane or sarcoplasmic reticulum. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.79).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.175 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
AKAP6	NM_004274.5	c.3588+6982G>A		intron_variant		ENST00000280979.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
AKAP6	ENST00000280979.9	c.3588+6982G>A		intron_variant		1	NM_004274.5	P1
AKAP6	ENST00000557272.1	c.3588+6982G>A		intron_variant		5

Frequencies

GnomAD3 genomes AF: 0.0953 AC: 14485 AN: 151926 Hom.: 747 Cov.: 32

Gnomad AFR AF: 0.0863

Gnomad AMI AF: 0.120

Gnomad AMR AF: 0.125

Gnomad ASJ AF: 0.0873

Gnomad EAS AF: 0.185

Gnomad SAS AF: 0.163

Gnomad FIN AF: 0.0800

Gnomad MID AF: 0.0860

Gnomad NFE AF: 0.0854

Gnomad OTH AF: 0.0889

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

GnomAD4 genome AF: 0.0953 AC: 14492 AN: 152044 Hom.: 746 Cov.: 32 AF XY: 0.0959 AC XY: 7129 AN XY: 74328

Gnomad4 AFR AF: 0.0863

Gnomad4 AMR AF: 0.124

Gnomad4 ASJ AF: 0.0873

Gnomad4 EAS AF: 0.185

Gnomad4 SAS AF: 0.164

Gnomad4 FIN AF: 0.0800

Gnomad4 NFE AF: 0.0854

Gnomad4 OTH AF: 0.0875

Alfa AF: 0.0922 Hom.: 372

Bravo AF: 0.0995

Asia WGS AF: 0.145 AC: 502 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.79
Cadd	Benign	1.1
Dann	Benign	0.61

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: rs10131032; hg19: chr14-33250081;