rs3767635

Positions:

• chr1-161851114-A-G

Variant summary

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

The NM_007348.4(ATF6):​c.1320-608A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.23 in 148,902 control chromosomes in the GnomAD database, including 5,178 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 0.23 (5178 hom., cov: 30)
• Consequence: ATF6 NM_007348.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.139

Genes affected

ATF6 (HGNC:791): (activating transcription factor 6) This gene encodes a transcription factor that activates target genes for the unfolded protein response (UPR) during endoplasmic reticulum (ER) stress. Although it is a transcription factor, this protein is unusual in that it is synthesized as a transmembrane protein that is embedded in the ER. It functions as an ER stress sensor/transducer, and following ER stress-induced proteolysis, it functions as a nuclear transcription factor via a cis-acting ER stress response element (ERSE) that is present in the promoters of genes encoding ER chaperones. This protein has been identified as a survival factor for quiescent but not proliferative squamous carcinoma cells. There have been conflicting reports about the association of polymorphisms in this gene with diabetes in different populations, but another polymorphism has been associated with increased plasma cholesterol levels. This gene is also thought to be a potential therapeutic target for cystic fibrosis. [provided by RefSeq, Aug 2011]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.81).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.343 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ATF6	NM_007348.4	c.1320-608A>G		intron_variant		ENST00000367942.4

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ATF6	ENST00000367942.4	c.1320-608A>G		intron_variant		1	NM_007348.4	A2

Frequencies

GnomAD3 genomes AF: 0.230 AC: 34207 AN: 148786 Hom.: 5176 Cov.: 30

Gnomad AFR AF: 0.0526

Gnomad AMI AF: 0.236

Gnomad AMR AF: 0.227

Gnomad ASJ AF: 0.420

Gnomad EAS AF: 0.0455

Gnomad SAS AF: 0.356

Gnomad FIN AF: 0.385

Gnomad MID AF: 0.356

Gnomad NFE AF: 0.309

Gnomad OTH AF: 0.264

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

GnomAD4 genome AF: 0.230 AC: 34206 AN: 148902 Hom.: 5178 Cov.: 30 AF XY: 0.233 AC XY: 16914 AN XY: 72544

Gnomad4 AFR AF: 0.0525

Gnomad4 AMR AF: 0.227

Gnomad4 ASJ AF: 0.420

Gnomad4 EAS AF: 0.0456

Gnomad4 SAS AF: 0.357

Gnomad4 FIN AF: 0.385

Gnomad4 NFE AF: 0.309

Gnomad4 OTH AF: 0.262

Alfa AF: 0.304 Hom.: 9920

Bravo AF: 0.210

Asia WGS AF: 0.165 AC: 561 AN: 3388

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.81
CADD	Benign	3.6
DANN	Benign	0.82

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: rs3767635; hg19: chr1-161820904;