rs10922573

Variant names:

• chr1-89122697-A-G
• rs10922573
• NM_004120.5:c.-17-714T>C

Your query was ambiguous. Multiple possible variants found:

• chr1-89122697-A-G
• chr1-89122697-A-T

Variant summary

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

The NM_004120.5(GBP2):​c.-17-714T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.398 in 151,988 control chromosomes in the GnomAD database, including 13,516 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 0.40 (13516 hom., cov: 32)
• Consequence: GBP2 NM_004120.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 1.01
• Publications: 10 publications found

Genes affected

GBP2 (HGNC:4183): (guanylate binding protein 2) This gene belongs to the guanine-binding protein (GBP) family, which includes interferon-induced proteins that can bind to guanine nucleotides (GMP, GDP and GTP). The encoded protein is a GTPase which hydrolyzes GTP, predominantly to GDP. The protein may play a role as a marker of squamous cell carcinomas. [provided by RefSeq, Jul 2013]

LOC112268267 (HGNC:):

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 (NFE) allele frequency at 95% confidence interval = 0.493 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
GBP2	NM_004120.5	c.-17-714T>C		intron_variant	Intron 1 of 10	ENST00000370466.4	NP_004111.2
LOC112268267	XR_007066213.1	n.4052A>G		non_coding_transcript_exon_variant	Exon 2 of 2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
GBP2	ENST00000370466.4	c.-17-714T>C		intron_variant	Intron 1 of 10	1	NM_004120.5	ENSP00000359497.3
GBP2	ENST00000464839.5	n.-17-714T>C		intron_variant	Intron 4 of 14	2		ENSP00000434282.1

Frequencies

GnomAD3 genomes AF: 0.398 AC: 60472 AN: 151870 Hom.: 13519 Cov.: 32

Gnomad AFR AF: 0.203

Gnomad AMI AF: 0.457

Gnomad AMR AF: 0.321

Gnomad ASJ AF: 0.411

Gnomad EAS AF: 0.398

Gnomad SAS AF: 0.486

Gnomad FIN AF: 0.583

Gnomad MID AF: 0.455

Gnomad NFE AF: 0.498

Gnomad OTH AF: 0.405

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

GnomAD4 genome AF: 0.398 AC: 60469 AN: 151988 Hom.: 13516 Cov.: 32 AF XY: 0.402 AC XY: 29888 AN XY: 74294

African (AFR) AF: 0.203 AC: 8400 AN: 41440

American (AMR) AF: 0.320 AC: 4891 AN: 15280

Ashkenazi Jewish (ASJ) AF: 0.411 AC: 1424 AN: 3466

East Asian (EAS) AF: 0.398 AC: 2059 AN: 5170

South Asian (SAS) AF: 0.487 AC: 2349 AN: 4828

European-Finnish (FIN) AF: 0.583 AC: 6148 AN: 10550

Middle Eastern (MID) AF: 0.449 AC: 131 AN: 292

European-Non Finnish (NFE) AF: 0.497 AC: 33801 AN: 67942

Other (OTH) AF: 0.403 AC: 849 AN: 2108

Alfa AF: 0.460 Hom.: 27221

Bravo AF: 0.366

Asia WGS AF: 0.408 AC: 1419 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
CADD	Benign	3.6
DANN	Benign	0.50
PhyloP100		1.0
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: rs10922573; hg19: chr1-89588380; COSMIC: COSV65068885; COSMIC: COSV65068885;