rs7292425

Variant names:

• chr22-44173534-C-A
• rs7292425
• ENST00000453888.7:n.208+343C>A

Your query was ambiguous. Multiple possible variants found:

• chr22-44173534-C-A
• chr22-44173534-C-G
• chr22-44173534-C-T

Variant summary

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

The NM_001137605.3(PARVG):​c.-189+343C>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.249 in 138,518 control chromosomes in the GnomAD database, including 4,095 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 0.25 (4095 hom., cov: 32)
• Consequence: PARVG NM_001137605.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.558
• Publications: 6 publications found

Genes affected

PARVG (HGNC:14654): (parvin gamma) Members of the parvin family, including PARVG, are actin-binding proteins associated with focal contacts.[supplied by OMIM, Aug 2004]

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 = 0.313 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001137605.3. 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
	PARVG	NM_001137605.3		c.-189+343C>A		intron	N/A	NP_001131077.1	Q9HBI0-1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	PARVG	ENST00000453888.7	TSL:1	n.208+343C>A		intron	N/A
	PARVG	ENST00000877232.1		c.-13+343C>A		intron	N/A	ENSP00000547291.1
	PARVG	ENST00000964876.1		c.-189+343C>A		intron	N/A	ENSP00000634935.1

Frequencies

GnomAD3 genomes AF: 0.249 AC: 34428 AN: 138406 Hom.: 4091 Cov.: 32

Gnomad AFR AF: 0.318

Gnomad AMI AF: 0.127

Gnomad AMR AF: 0.186

Gnomad ASJ AF: 0.285

Gnomad EAS AF: 0.189

Gnomad SAS AF: 0.186

Gnomad FIN AF: 0.295

Gnomad MID AF: 0.295

Gnomad NFE AF: 0.228

Gnomad OTH AF: 0.239

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

GnomAD4 genome AF: 0.249 AC: 34449 AN: 138518 Hom.: 4095 Cov.: 32 AF XY: 0.247 AC XY: 16776 AN XY: 67912

African (AFR) AF: 0.318 AC: 10959 AN: 34438

American (AMR) AF: 0.185 AC: 2671 AN: 14402

Ashkenazi Jewish (ASJ) AF: 0.285 AC: 946 AN: 3322

East Asian (EAS) AF: 0.188 AC: 967 AN: 5142

South Asian (SAS) AF: 0.185 AC: 875 AN: 4718

European-Finnish (FIN) AF: 0.295 AC: 2957 AN: 10040

Middle Eastern (MID) AF: 0.285 AC: 78 AN: 274

European-Non Finnish (NFE) AF: 0.228 AC: 14427 AN: 63412

Other (OTH) AF: 0.239 AC: 463 AN: 1936

Alfa AF: 0.210 Hom.: 3471

Bravo AF: 0.221

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.90
CADD	Benign	0.25
DANN	Benign	0.52
PhyloP100		-0.56
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

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

Other links and lift over

dbSNP: rs7292425;

hg19: chr22-44569414;