rs7425883

Variant names:

• chr2-97715058-G-C
• rs7425883
• NM_001079.4:c.-22+1064G>C

Your query was ambiguous. Multiple possible variants found:

• chr2-97715058-G-C
• chr2-97715058-G-T

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_001079.4(ZAP70):​c.-22+1064G>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.186 in 152,108 control chromosomes in the GnomAD database, including 2,909 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 0.19 (2909 hom., cov: 32)
• Consequence: ZAP70 NM_001079.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.121

Genes affected

ZAP70 (HGNC:12858): (zeta chain of T cell receptor associated protein kinase 70) This gene encodes an enzyme belonging to the protein tyrosine kinase family, and it plays a role in T-cell development and lymphocyte activation. This enzyme, which is phosphorylated on tyrosine residues upon T-cell antigen receptor (TCR) stimulation, functions in the initial step of TCR-mediated signal transduction in combination with the Src family kinases, Lck and Fyn. This enzyme is also essential for thymocyte development. Mutations in this gene cause selective T-cell defect, a severe combined immunodeficiency disease characterized by a selective absence of CD8-positive T-cells. Two transcript variants that encode different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.95).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.216 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
ZAP70	NM_001079.4	c.-22+1064G>C		intron_variant	Intron 2 of 13	ENST00000264972.10	NP_001070.2

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
ZAP70	ENST00000264972.10	c.-22+1064G>C		intron_variant	Intron 2 of 13	1	NM_001079.4	ENSP00000264972.5
ZAP70	ENST00000698508.1	c.-22+1064G>C		intron_variant	Intron 1 of 12			ENSP00000513759.1
ZAP70	ENST00000483781.5	n.172+1064G>C		intron_variant	Intron 2 of 6	2

Frequencies

GnomAD3 genomes AF: 0.186 AC: 28344 AN: 151990 Hom.: 2910 Cov.: 32

Gnomad AFR AF: 0.157

Gnomad AMI AF: 0.316

Gnomad AMR AF: 0.206

Gnomad ASJ AF: 0.218

Gnomad EAS AF: 0.0993

Gnomad SAS AF: 0.0742

Gnomad FIN AF: 0.120

Gnomad MID AF: 0.301

Gnomad NFE AF: 0.219

Gnomad OTH AF: 0.240

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

GnomAD4 genome AF: 0.186 AC: 28346 AN: 152108 Hom.: 2909 Cov.: 32 AF XY: 0.181 AC XY: 13459 AN XY: 74366

Gnomad4 AFR AF: 0.157

Gnomad4 AMR AF: 0.206

Gnomad4 ASJ AF: 0.218

Gnomad4 EAS AF: 0.0993

Gnomad4 SAS AF: 0.0740

Gnomad4 FIN AF: 0.120

Gnomad4 NFE AF: 0.219

Gnomad4 OTH AF: 0.238

Alfa AF: 0.0957 Hom.: 142

Bravo AF: 0.193

Asia WGS AF: 0.135 AC: 472 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.95
CADD	Benign	2.2
DANN	Benign	0.37

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.040		Details are displayed if max score is > 0.2

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

Publications

LitVar

Other links and lift over

dbSNP: rs7425883; hg19: chr2-98331521;