1-192750241-G-A

Variant names:

• chr1-192750241-G-A
• rs10489516
• ENST00000644058.2:n.505+14567C>T

Variant summary

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

The ENST00000644058.2(RGS2-AS1):​n.505+14567C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.159 in 152,114 control chromosomes in the GnomAD database, including 4,124 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 0.16 (4124 hom., cov: 32)
• Consequence: RGS2-AS1 ENST00000644058.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.335
• Publications: 0 publications found

Genes affected

RGS2-AS1 (HGNC:49018): (RSG2 antisense RNA 1)

ENSG00000296235 (HGNC:):

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.9).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.421 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000644058.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RGS2-AS1	ENST00000644058.2		n.505+14567C>T		intron	N/A
	RGS2-AS1	ENST00000644134.1		n.408+14567C>T		intron	N/A
	RGS2-AS1	ENST00000645822.1		n.673+14567C>T		intron	N/A

Frequencies

GnomAD3 genomes AF: 0.159 AC: 24192 AN: 151996 Hom.: 4104 Cov.: 32

Gnomad AFR AF: 0.425

Gnomad AMI AF: 0.0406

Gnomad AMR AF: 0.141

Gnomad ASJ AF: 0.0956

Gnomad EAS AF: 0.0626

Gnomad SAS AF: 0.170

Gnomad FIN AF: 0.0103

Gnomad MID AF: 0.127

Gnomad NFE AF: 0.0367

Gnomad OTH AF: 0.140

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

GnomAD4 genome AF: 0.159 AC: 24262 AN: 152114 Hom.: 4124 Cov.: 32 AF XY: 0.160 AC XY: 11880 AN XY: 74406

African (AFR) AF: 0.426 AC: 17648 AN: 41450

American (AMR) AF: 0.141 AC: 2162 AN: 15284

Ashkenazi Jewish (ASJ) AF: 0.0956 AC: 332 AN: 3472

East Asian (EAS) AF: 0.0624 AC: 323 AN: 5178

South Asian (SAS) AF: 0.170 AC: 818 AN: 4820

European-Finnish (FIN) AF: 0.0103 AC: 109 AN: 10604

Middle Eastern (MID) AF: 0.122 AC: 36 AN: 294

European-Non Finnish (NFE) AF: 0.0368 AC: 2499 AN: 67990

Other (OTH) AF: 0.141 AC: 298 AN: 2110

Alfa AF: 0.110 Hom.: 861

Bravo AF: 0.179

Asia WGS AF: 0.132 AC: 455 AN: 3462

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	5.9
DANN	Benign	0.41
PhyloP100		0.34

Splicing

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

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs10489516;

hg19: chr1-192719371;