rs9293329

Positions:

• chr5-83100768-G-A

Variant summary

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

The NM_003401.5(XRCC4):​c.-10-4142G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0717 in 147,408 control chromosomes in the GnomAD database, including 545 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 0.072 (545 hom., cov: 32)
• Consequence: XRCC4 NM_003401.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.371

Genes affected

XRCC4 (HGNC:12831): (X-ray repair cross complementing 4) The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternate transcript variants such as NM_022406 are unlikely to be expressed in some individuals due to a polymorphism (rs1805377) in the last splice acceptor site. [provided by RefSeq, Oct 2019]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.88).
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.103 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
XRCC4	NM_003401.5	c.-10-4142G>A		intron_variant		ENST00000396027.9

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
XRCC4	ENST00000396027.9	c.-10-4142G>A		intron_variant		5	NM_003401.5	A1

Frequencies

GnomAD3 genomes AF: 0.0718 AC: 10574 AN: 147290 Hom.: 546 Cov.: 32

Gnomad AFR AF: 0.0165

Gnomad AMI AF: 0.0528

Gnomad AMR AF: 0.0381

Gnomad ASJ AF: 0.0353

Gnomad EAS AF: 0.00116

Gnomad SAS AF: 0.0291

Gnomad FIN AF: 0.200

Gnomad MID AF: 0.0321

Gnomad NFE AF: 0.105

Gnomad OTH AF: 0.0495

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

GnomAD4 genome AF: 0.0717 AC: 10573 AN: 147408 Hom.: 545 Cov.: 32 AF XY: 0.0737 AC XY: 5303 AN XY: 71960

Gnomad4 AFR AF: 0.0165

Gnomad4 AMR AF: 0.0382

Gnomad4 ASJ AF: 0.0353

Gnomad4 EAS AF: 0.000969

Gnomad4 SAS AF: 0.0289

Gnomad4 FIN AF: 0.200

Gnomad4 NFE AF: 0.105

Gnomad4 OTH AF: 0.0490

Alfa AF: 0.0894 Hom.: 371

Bravo AF: 0.0555

Asia WGS AF: 0.0120 AC: 41 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.88
CADD	Benign	1.8
DANN	Benign	0.16

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

Publications

LitVar

Other links and lift over

dbSNP: rs9293329; hg19: chr5-82396587;