rs10517025

chr4-42451236-C-T

Variant summary

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

The NM_006095.2(ATP8A1):c.2896+745G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.154 in 152,080 control chromosomes in the GnomAD database, including 2,218 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 0.15 (2218 hom., cov: 31)
• Consequence: ATP8A1 NM_006095.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.13

Genes affected

ATP8A1 (HGNC:13531): (ATPase phospholipid transporting 8A1) The P-type adenosinetriphosphatases (P-type ATPases) are a family of proteins which use the free energy of ATP hydrolysis to drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily catalyzes transport of heavy metal ions. Another subfamily transports non-heavy metal ions (NMHI). The protein encoded by this gene is a member of the third subfamily of P-type ATPases and acts to transport amphipaths, such as phosphatidylserine. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.225 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ATP8A1	NM_006095.2	c.2896+745G>A		intron_variant		ENST00000381668.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ATP8A1	ENST00000381668.9	c.2896+745G>A		intron_variant		1	NM_006095.2	A1

Frequencies

GnomAD3 genomes AF: 0.154 AC: 23359 AN: 151960 Hom.: 2220 Cov.: 31

Gnomad AFR AF: 0.0381

Gnomad AMI AF: 0.267

Gnomad AMR AF: 0.188

Gnomad ASJ AF: 0.169

Gnomad EAS AF: 0.226

Gnomad SAS AF: 0.237

Gnomad FIN AF: 0.151

Gnomad MID AF: 0.175

Gnomad NFE AF: 0.203

Gnomad OTH AF: 0.157

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

GnomAD4 genome AF: 0.154 AC: 23355 AN: 152080 Hom.: 2218 Cov.: 31 AF XY: 0.153 AC XY: 11396 AN XY: 74316

Gnomad4 AFR AF: 0.0381

Gnomad4 AMR AF: 0.188

Gnomad4 ASJ AF: 0.169

Gnomad4 EAS AF: 0.226

Gnomad4 SAS AF: 0.237

Gnomad4 FIN AF: 0.151

Gnomad4 NFE AF: 0.203

Gnomad4 OTH AF: 0.157

Alfa AF: 0.194 Hom.: 3649

Bravo AF: 0.147

Asia WGS AF: 0.206 AC: 716 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
Cadd	Benign	3.3
Dann	Benign	0.63

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: rs10517025; hg19: chr4-42453253;