chr10-48602322-G-T

Variant names:

• chr10-48602322-G-T
• rs10491034
• NM_021226.4:c.34+2441C>A

Variant summary

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

The NM_021226.4(ARHGAP22):​c.34+2441C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0227 in 152,162 control chromosomes in the GnomAD database, including 114 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 0.023 (114 hom., cov: 32)
• Consequence: ARHGAP22 NM_021226.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.11
• Publications: 2 publications found

Genes affected

ARHGAP22 (HGNC:30320): (Rho GTPase activating protein 22) This gene encodes a member of the GTPase activating protein family which activates a GTPase belonging to the RAS superfamily of small GTP-binding proteins. The encoded protein is insulin-responsive, is dependent on the kinase Akt and requires the Akt-dependent 14-3-3 binding protein which binds sequentially to two serine residues. The result of these interactions is regulation of cell motility. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

ACMG classification

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

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.99).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.121 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_021226.4. 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
	ARHGAP22	NM_021226.4	MANE Select	c.34+2441C>A		intron	N/A	NP_067049.2
	ARHGAP22	NM_001256024.2		c.34+2441C>A		intron	N/A	NP_001242953.1	Q7Z5H3-2
	ARHGAP22	NM_001256025.3		c.53-19170C>A		intron	N/A	NP_001242954.1	Q7Z5H3-5

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ARHGAP22	ENST00000249601.9	TSL:1 MANE Select	c.34+2441C>A		intron	N/A	ENSP00000249601.4	Q7Z5H3-1
	ARHGAP22	ENST00000417912.6	TSL:1	c.34+2441C>A		intron	N/A	ENSP00000412461.2	Q7Z5H3-2
	ARHGAP22	ENST00000435790.6	TSL:2	c.53-19170C>A		intron	N/A	ENSP00000416701.2	Q7Z5H3-5

Frequencies

GnomAD3 genomes AF: 0.0226 AC: 3443 AN: 152044 Hom.: 113 Cov.: 32

Gnomad AFR AF: 0.0251

Gnomad AMI AF: 0.00

Gnomad AMR AF: 0.0423

Gnomad ASJ AF: 0.0179

Gnomad EAS AF: 0.129

Gnomad SAS AF: 0.127

Gnomad FIN AF: 0.00728

Gnomad MID AF: 0.0127

Gnomad NFE AF: 0.00401

Gnomad OTH AF: 0.0292

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

GnomAD4 genome AF: 0.0227 AC: 3461 AN: 152162 Hom.: 114 Cov.: 32 AF XY: 0.0251 AC XY: 1864 AN XY: 74374

African (AFR) AF: 0.0253 AC: 1048 AN: 41500

American (AMR) AF: 0.0426 AC: 651 AN: 15290

Ashkenazi Jewish (ASJ) AF: 0.0179 AC: 62 AN: 3472

East Asian (EAS) AF: 0.130 AC: 671 AN: 5178

South Asian (SAS) AF: 0.127 AC: 611 AN: 4810

European-Finnish (FIN) AF: 0.00728 AC: 77 AN: 10580

Middle Eastern (MID) AF: 0.0136 AC: 4 AN: 294

European-Non Finnish (NFE) AF: 0.00401 AC: 273 AN: 68014

Other (OTH) AF: 0.0303 AC: 64 AN: 2112

Alfa AF: 0.00618 Hom.: 3

Bravo AF: 0.0263

Asia WGS AF: 0.138 AC: 478 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.99
CADD	Benign	0.35
DANN	Benign	0.70
PhyloP100		-1.1
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: rs10491034; hg19: chr10-49810367;