rs11858338

Positions:

• chr15-40716115-G-A

Variant summary

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

The NM_002875.5(RAD51):​c.436-2690G>A variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.493 in 152,048 control chromosomes in the GnomAD database, including 19,281 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 0.49 (19281 hom., cov: 33)
• Consequence: RAD51 NM_002875.5 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.487

Genes affected

RAD51 (HGNC:9817): (RAD51 recombinase) The protein encoded by this gene is a member of the RAD51 protein family. RAD51 family members are highly similar to bacterial RecA and Saccharomyces cerevisiae Rad51, and are known to be involved in the homologous recombination and repair of DNA. This protein can interact with the ssDNA-binding protein RPA and RAD52, and it is thought to play roles in homologous pairing and strand transfer of DNA. This protein is also found to interact with BRCA1 and BRCA2, which may be important for the cellular response to DNA damage. BRCA2 is shown to regulate both the intracellular localization and DNA-binding ability of this protein. Loss of these controls following BRCA2 inactivation may be a key event leading to genomic instability and tumorigenesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2009]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.96).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.753 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
RAD51	NM_002875.5	c.436-2690G>A		intron_variant		ENST00000267868.8

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
RAD51	ENST00000267868.8	c.436-2690G>A		intron_variant		1	NM_002875.5	P1

Frequencies

GnomAD3 genomes AF: 0.493 AC: 74847 AN: 151930 Hom.: 19264 Cov.: 33

Gnomad AFR AF: 0.365

Gnomad AMI AF: 0.452

Gnomad AMR AF: 0.599

Gnomad ASJ AF: 0.563

Gnomad EAS AF: 0.771

Gnomad SAS AF: 0.650

Gnomad FIN AF: 0.586

Gnomad MID AF: 0.503

Gnomad NFE AF: 0.497

Gnomad OTH AF: 0.491

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

GnomAD4 genome AF: 0.493 AC: 74889 AN: 152048 Hom.: 19281 Cov.: 33 AF XY: 0.503 AC XY: 37389 AN XY: 74296

Gnomad4 AFR AF: 0.364

Gnomad4 AMR AF: 0.600

Gnomad4 ASJ AF: 0.563

Gnomad4 EAS AF: 0.772

Gnomad4 SAS AF: 0.649

Gnomad4 FIN AF: 0.586

Gnomad4 NFE AF: 0.497

Gnomad4 OTH AF: 0.495

Alfa AF: 0.493 Hom.: 2302

Bravo AF: 0.491

Asia WGS AF: 0.708 AC: 2464 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.96
CADD	Benign	1.1
DANN	Benign	0.67

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: rs11858338; hg19: chr15-41008313;