chr9-86958168-G-A

Variant names:

• chr9-86958168-G-A
• rs9792548
• ENST00000415801.1:n.428+7169G>A

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The ENST00000415801.1(GAS1RR):​n.428+7169G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.528 in 152,030 control chromosomes in the GnomAD database, including 23,929 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 0.53 (23929 hom., cov: 33)
• Consequence: GAS1RR ENST00000415801.1 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -2.38
• Publications: 6 publications found

Genes affected

GAS1RR (HGNC:52261): (GAS1 adjacent regulatory RNA)

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.821 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000415801.1. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GAS1RR	NR_049794.1		n.429+7169G>A		intron	N/A

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	GAS1RR	ENST00000415801.1	TSL:1	n.428+7169G>A		intron	N/A
	GAS1RR	ENST00000701854.2		n.354+9175G>A		intron	N/A
	GAS1RR	ENST00000846239.1		n.307+9175G>A		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.528 AC: 80218 AN: 151912 Hom.: 23872 Cov.: 33

Gnomad AFR AF: 0.828

Gnomad AMI AF: 0.360

Gnomad AMR AF: 0.492

Gnomad ASJ AF: 0.422

Gnomad EAS AF: 0.493

Gnomad SAS AF: 0.409

Gnomad FIN AF: 0.420

Gnomad MID AF: 0.532

Gnomad NFE AF: 0.390

Gnomad OTH AF: 0.503

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

GnomAD4 genome AF: 0.528 AC: 80338 AN: 152030 Hom.: 23929 Cov.: 33 AF XY: 0.529 AC XY: 39341 AN XY: 74308

African (AFR) AF: 0.828 AC: 34365 AN: 41500

American (AMR) AF: 0.492 AC: 7512 AN: 15272

Ashkenazi Jewish (ASJ) AF: 0.422 AC: 1465 AN: 3468

East Asian (EAS) AF: 0.492 AC: 2546 AN: 5170

South Asian (SAS) AF: 0.411 AC: 1986 AN: 4830

European-Finnish (FIN) AF: 0.420 AC: 4424 AN: 10522

Middle Eastern (MID) AF: 0.544 AC: 160 AN: 294

European-Non Finnish (NFE) AF: 0.390 AC: 26494 AN: 67952

Other (OTH) AF: 0.501 AC: 1058 AN: 2112

Alfa AF: 0.444 Hom.: 40297

Bravo AF: 0.548

Asia WGS AF: 0.468 AC: 1630 AN: 3476

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	0.013
DANN	Benign	0.64
PhyloP100		-2.4

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs9792548; hg19: chr9-89573083;