rs10489965

Variant names:

• chr1-182654144-T-A
• rs10489965
• NM_001102450.3:c.194-5841A>T

Your query was ambiguous. Multiple possible variants found:

• chr1-182654144-T-A
• chr1-182654144-T-C
• chr1-182654144-T-G

Variant summary

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

The NM_001102450.3(RGS8):​c.194-5841A>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.674 in 152,088 control chromosomes in the GnomAD database, including 35,326 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 0.67 (35326 hom., cov: 32)
• Consequence: RGS8 NM_001102450.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.317
• Publications: 2 publications found

Genes affected

RGS8 (HGNC:16810): (regulator of G protein signaling 8) This gene is a member of the regulator of G protein signaling (RGS) family and encodes a protein with a single RGS domain. Regulator of G protein signaling (RGS) proteins are regulatory and structural components of G protein-coupled receptor complexes. They accelerate transit through the cycle of GTP binding and hydrolysis to GDP, thereby terminating signal transduction, but paradoxically, also accelerate receptor-stimulated activation. [provided by RefSeq, Jul 2008]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.746 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RGS8	NM_001102450.3	c.194-5841A>T		intron_variant	Intron 6 of 7	ENST00000515211.2	NP_001095920.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RGS8	ENST00000515211.2	c.194-5841A>T		intron_variant	Intron 6 of 7	4	NM_001102450.3	ENSP00000511884.1

Frequencies

GnomAD3 genomes AF: 0.675 AC: 102524 AN: 151968 Hom.: 35327 Cov.: 32

Gnomad AFR AF: 0.538

Gnomad AMI AF: 0.743

Gnomad AMR AF: 0.644

Gnomad ASJ AF: 0.634

Gnomad EAS AF: 0.608

Gnomad SAS AF: 0.731

Gnomad FIN AF: 0.779

Gnomad MID AF: 0.633

Gnomad NFE AF: 0.751

Gnomad OTH AF: 0.662

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

GnomAD4 genome AF: 0.674 AC: 102553 AN: 152088 Hom.: 35326 Cov.: 32 AF XY: 0.674 AC XY: 50130 AN XY: 74348

African (AFR) AF: 0.537 AC: 22250 AN: 41442

American (AMR) AF: 0.644 AC: 9843 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.634 AC: 2199 AN: 3470

East Asian (EAS) AF: 0.609 AC: 3154 AN: 5182

South Asian (SAS) AF: 0.731 AC: 3520 AN: 4814

European-Finnish (FIN) AF: 0.779 AC: 8245 AN: 10580

Middle Eastern (MID) AF: 0.609 AC: 179 AN: 294

European-Non Finnish (NFE) AF: 0.751 AC: 51084 AN: 67990

Other (OTH) AF: 0.663 AC: 1401 AN: 2114

Alfa AF: 0.710 Hom.: 4862

Bravo AF: 0.653

Asia WGS AF: 0.696 AC: 2421 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
CADD	Benign	2.5
DANN	Benign	0.80
PhyloP100		-0.32
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs10489965; hg19: chr1-182623279; COSMIC: COSV51119882; COSMIC: COSV51119882;