12-121631099-T-G

Variant names:

• chr12-121631099-T-G
• rs7135617
• ENST00000617316.2:c.303+4049T>G

Variant summary

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

The ENST00000617316.2(ORAI1):​c.303+4049T>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.57 in 152,100 control chromosomes in the GnomAD database, including 27,836 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 0.57 (27836 hom., cov: 32)
• Consequence: ORAI1 ENST00000617316.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.411

Genes affected

ORAI1 (HGNC:25896): (ORAI calcium release-activated calcium modulator 1) The protein encoded by this gene is a membrane calcium channel subunit that is activated by the calcium sensor STIM1 when calcium stores are depleted. This type of channel is the primary way for calcium influx into T-cells. Defects in this gene are a cause of immune dysfunction with T-cell inactivation due to calcium entry defect type 1 (IDTICED1). [provided by RefSeq, Sep 2011]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.73).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.881 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ORAI1	NR_186857.1	n.521+4049T>G		intron_variant	Intron 1 of 1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ORAI1	ENST00000617316.2	c.303+4049T>G		intron_variant	Intron 2 of 2	1		ENSP00000482568.2
ORAI1	ENST00000611718.1	n.359+3925T>G		intron_variant	Intron 1 of 1	5
ORAI1	ENST00000646827.1	n.501+4049T>G		intron_variant	Intron 1 of 1
ORAI1	ENST00000698901.1	n.425+4166T>G		intron_variant	Intron 1 of 1

Frequencies

GnomAD3 genomes AF: 0.569 AC: 86502 AN: 151982 Hom.: 27772 Cov.: 32

Gnomad AFR AF: 0.888

Gnomad AMI AF: 0.407

Gnomad AMR AF: 0.504

Gnomad ASJ AF: 0.378

Gnomad EAS AF: 0.596

Gnomad SAS AF: 0.518

Gnomad FIN AF: 0.447

Gnomad MID AF: 0.424

Gnomad NFE AF: 0.424

Gnomad OTH AF: 0.527

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

GnomAD4 genome AF: 0.570 AC: 86637 AN: 152100 Hom.: 27836 Cov.: 32 AF XY: 0.568 AC XY: 42201 AN XY: 74338

Gnomad4 AFR AF: 0.889

Gnomad4 AMR AF: 0.504

Gnomad4 ASJ AF: 0.378

Gnomad4 EAS AF: 0.597

Gnomad4 SAS AF: 0.518

Gnomad4 FIN AF: 0.447

Gnomad4 NFE AF: 0.424

Gnomad4 OTH AF: 0.527

Alfa AF: 0.430 Hom.: 6861

Bravo AF: 0.588

Asia WGS AF: 0.597 AC: 2078 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.73
CADD	Benign	14
DANN	Benign	0.66

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: rs7135617; hg19: chr12-122069005;