Variant chr11-47238768-A-G details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Benign. Variant got -20 ACMG points: 0P and 20B. BP4_StrongBP6_Very_StrongBA1

The ENST00000256996.9(DDB2):c.1235-32A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.343 in 1,610,664 control chromosomes in the GnomAD database, including 103,621 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

Frequency

Genomes: 𝑓 0.41 ( 13973 hom., cov: 30)

Exomes 𝑓: 0.34 ( 89648 hom. )

Consequence

DDB2
ENST00000256996.9 intron

Scores

Clinical Significance

Benign criteria provided, multiple submitters, no conflicts B:3

Conservation

PhyloP100: -0.552

Variant links:

Genes affected

DDB2 (HGNC:2718): (damage specific DNA binding protein 2) This gene encodes a protein that is necessary for the repair of ultraviolet light-damaged DNA. This protein is the smaller subunit of a heterodimeric protein complex that participates in nucleotide excision repair, and this complex mediates the ubiquitylation of histones H3 and H4, which facilitates the cellular response to DNA damage. This subunit appears to be required for DNA binding. Mutations in this gene cause xeroderma pigmentosum complementation group E, a recessive disease that is characterized by an increased sensitivity to UV light and a high predisposition for skin cancer development, in some cases accompanied by neurological abnormalities. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]

DDB2 links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -20 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.9).

BP6

Variant 11-47238768-A-G is Benign according to our data. Variant chr11-47238768-A-G is described in ClinVar as [Benign]. Clinvar id is 1182792.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BA1

GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.73 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
DDB2	NM_000107.3 linkuse as main transcript	c.1235-32A>G		intron_variant		ENST00000256996.9	NP_000098.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
DDB2	ENST00000256996.9 linkuse as main transcript	c.1235-32A>G		intron_variant		1	NM_000107.3	ENSP00000256996	P1	Q92466-1

Frequencies

GnomAD3 genomes

AF:

0.407

AC:

61569

AN:

151438

Hom.:

13959

Cov.:

show subpopulations

Gnomad AFR

AF:

0.570

Gnomad AMI

AF:

0.133

Gnomad AMR

AF:

0.365

Gnomad ASJ

AF:

0.224

Gnomad EAS

AF:

0.750

Gnomad SAS

AF:

0.467

Gnomad FIN

AF:

0.427

Gnomad MID

AF:

0.263

Gnomad NFE

AF:

0.299

Gnomad OTH

AF:

0.344

GnomAD3 exomes

AF:

0.397

AC:

98939

AN:

249526

Hom.:

22181

AF XY:

0.387

AC XY:

52297

AN XY:

135018

show subpopulations

Gnomad AFR exome

AF:

0.578

Gnomad AMR exome

AF:

0.441

Gnomad ASJ exome

AF:

0.218

Gnomad EAS exome

AF:

0.758

Gnomad SAS exome

AF:

0.462

Gnomad FIN exome

AF:

0.418

Gnomad NFE exome

AF:

0.296

Gnomad OTH exome

AF:

0.321

GnomAD4 exome

AF:

0.336

AC:

490310

AN:

1459106

Hom.:

89648

Cov.:

AF XY:

0.337

AC XY:

244969

AN XY:

726006

show subpopulations

Gnomad4 AFR exome

AF:

0.574

Gnomad4 AMR exome

AF:

0.429

Gnomad4 ASJ exome

AF:

0.218

Gnomad4 EAS exome

AF:

0.742

Gnomad4 SAS exome

AF:

0.461

Gnomad4 FIN exome

AF:

0.409

Gnomad4 NFE exome

AF:

0.300

Gnomad4 OTH exome

AF:

0.346

GnomAD4 genome

AF:

0.407

AC:

61617

AN:

151558

Hom.:

13973

Cov.:

AF XY:

0.416

AC XY:

30798

AN XY:

74016

show subpopulations

Gnomad4 AFR

AF:

0.570

Gnomad4 AMR

AF:

0.365

Gnomad4 ASJ

AF:

0.224

Gnomad4 EAS

AF:

0.750

Gnomad4 SAS

AF:

0.467

Gnomad4 FIN

AF:

0.427

Gnomad4 NFE

AF:

0.299

Gnomad4 OTH

AF:

0.340

Alfa

AF:

0.304

Hom.:

7895

Bravo

AF:

0.408

Asia WGS

AF:

0.550

AC:

1909

AN:

3478

ClinVar

Significance: Benign

Submissions summary: Benign:3

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:2

Benign, criteria provided, single submitter	not provided	Breakthrough Genomics, Breakthrough Genomics	-	- -
Benign, criteria provided, single submitter	clinical testing	GeneDx	Feb 02, 2019	- -

Xeroderma pigmentosum, group E

Benign:1

Benign, criteria provided, single submitter

clinical testing

Genome-Nilou Lab

Jul 30, 2021

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.90

CADD

Benign

2.5

DANN

Benign

0.53

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.010

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

Below is the list of publications found by LitVar. It may be empty.

Variant summary

Frequency

Consequence

Scores

Clinical Significance

Conservation

ACMG classification

Transcripts

RefSeq

Ensembl

Frequencies

ClinVar

Submissions by phenotype

Computational scores

Splicing

Publications

LitVar

Other links and lift over