rs3218461

Positions:

• chr7-152662734-G-A

Variant summary

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

The NM_005431.2(XRCC2):​c.40-1952C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.26 in 150,328 control chromosomes in the GnomAD database, including 5,203 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 0.26 (5203 hom., cov: 26)
• Consequence: XRCC2 NM_005431.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.438

Genes affected

XRCC2 (HGNC:12829): (X-ray repair cross complementing 2) This gene encodes a member of the RecA/Rad51-related protein family that participates in homologous recombination to maintain chromosome stability and repair DNA damage. This gene is involved in the repair of DNA double-strand breaks by homologous recombination and it functionally complements Chinese hamster irs1, a repair-deficient mutant that exhibits hypersensitivity to a number of different DNA-damaging agents. [provided by RefSeq, Jul 2008]

XRCC2 (HGNC:):

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.91).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.305 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
XRCC2	NM_005431.2	c.40-1952C>T		intron_variant		ENST00000359321.2	NP_005422.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
XRCC2	ENST00000359321.2	c.40-1952C>T		intron_variant		1	NM_005431.2	ENSP00000352271.1
XRCC2	ENST00000495707.1	n.61+1210C>T		intron_variant		1
XRCC2	ENST00000698506.1	c.-48+13307C>T		intron_variant				ENSP00000513758.1
XRCC2	ENST00000698507.1	n.108-1952C>T		intron_variant

Frequencies

GnomAD3 genomes AF: 0.260 AC: 39073 AN: 150210 Hom.: 5197 Cov.: 26

Gnomad AFR AF: 0.286

Gnomad AMI AF: 0.0695

Gnomad AMR AF: 0.200

Gnomad ASJ AF: 0.202

Gnomad EAS AF: 0.276

Gnomad SAS AF: 0.319

Gnomad FIN AF: 0.246

Gnomad MID AF: 0.242

Gnomad NFE AF: 0.261

Gnomad OTH AF: 0.238

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

GnomAD4 genome AF: 0.260 AC: 39099 AN: 150328 Hom.: 5203 Cov.: 26 AF XY: 0.259 AC XY: 19008 AN XY: 73310

Gnomad4 AFR AF: 0.286

Gnomad4 AMR AF: 0.199

Gnomad4 ASJ AF: 0.202

Gnomad4 EAS AF: 0.276

Gnomad4 SAS AF: 0.318

Gnomad4 FIN AF: 0.246

Gnomad4 NFE AF: 0.261

Gnomad4 OTH AF: 0.238

Alfa AF: 0.251 Hom.: 485

Bravo AF: 0.256

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.91
CADD	Benign	3.4
DANN	Benign	0.96

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: rs3218461; hg19: chr7-152359819;