rs12726081

chr1-26711084-A-G

Variant summary

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

The NM_006015.6(ARID1A):c.1137+13544A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.06 in 150,070 control chromosomes in the GnomAD database, including 320 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 0.060 (320 hom., cov: 31)
• Consequence: ARID1A NM_006015.6 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.41

Genes affected

ARID1A (HGNC:11110): (AT-rich interaction domain 1A) This gene encodes a member of the SWI/SNF family, whose members have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. It possesses at least two conserved domains that could be important for its function. First, it has a DNA-binding domain that can specifically bind an AT-rich DNA sequence known to be recognized by a SNF/SWI complex at the beta-globin locus. Second, the C-terminus of the protein can stimulate glucocorticoid receptor-dependent transcriptional activation. It is thought that the protein encoded by this gene confers specificity to the SNF/SWI complex and may recruit the complex to its targets through either protein-DNA or protein-protein interactions. 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=-0.94).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.0783 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
ARID1A	NM_006015.6	c.1137+13544A>G		intron_variant		ENST00000324856.13
ARID1A	NM_139135.4	c.1137+13544A>G		intron_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
ARID1A	ENST00000324856.13	c.1137+13544A>G		intron_variant		1	NM_006015.6
ARID1A	ENST00000430799.7	c.-13+17467A>G		intron_variant		5		A2
ARID1A	ENST00000457599.6	c.1137+13544A>G		intron_variant		5
ARID1A	ENST00000637465.1	c.-13+14984A>G		intron_variant		5

Frequencies

GnomAD3 genomes AF: 0.0600 AC: 9005 AN: 150026 Hom.: 319 Cov.: 31

Gnomad AFR AF: 0.0293

Gnomad AMI AF: 0.0592

Gnomad AMR AF: 0.0557

Gnomad ASJ AF: 0.0503

Gnomad EAS AF: 0.0196

Gnomad SAS AF: 0.0488

Gnomad FIN AF: 0.0880

Gnomad MID AF: 0.0455

Gnomad NFE AF: 0.0801

Gnomad OTH AF: 0.0559

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

GnomAD4 genome AF: 0.0600 AC: 9009 AN: 150070 Hom.: 320 Cov.: 31 AF XY: 0.0595 AC XY: 4357 AN XY: 73190

Gnomad4 AFR AF: 0.0294

Gnomad4 AMR AF: 0.0556

Gnomad4 ASJ AF: 0.0503

Gnomad4 EAS AF: 0.0195

Gnomad4 SAS AF: 0.0492

Gnomad4 FIN AF: 0.0880

Gnomad4 NFE AF: 0.0801

Gnomad4 OTH AF: 0.0556

Alfa AF: 0.0663 Hom.: 58

Bravo AF: 0.0556

Asia WGS AF: 0.0400 AC: 138 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
Cadd	Benign	1.8
Dann	Benign	0.14

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: rs12726081; hg19: chr1-27037575;