Variant chr6-33195674-G-A details in Genebe, Genetics Data Aggregator

Variant summary

Our verdict is Benign. Variant got -15 ACMG points: 0P and 15B. BP4_StrongBP6_ModerateBP7BA1

The NM_021976.5(RXRB):c.1152C>T(p.Phe384=) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.74 in 1,612,344 control chromosomes in the GnomAD database, including 444,715 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

Frequency

Genomes: 𝑓 0.77 ( 45628 hom., cov: 32)

Exomes 𝑓: 0.74 ( 399087 hom. )

Consequence

RXRB
NM_021976.5 synonymous

Scores

Clinical Significance

Benign criteria provided, single submitter B:2

Conservation

PhyloP100: 2.99

Variant links:

Genes affected

RXRB (HGNC:10478): (retinoid X receptor beta) This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the effects of retinoic acid (RA). The encoded protein forms homodimers with the retinoic acid, thyroid hormone, and vitamin D receptors, increasing both DNA binding and transcriptional function on their respective response elements. This gene lies within the major histocompatibility complex (MHC) class II region on chromosome 6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012]

RXRB links:

Genome browser will be placed here

ACMG classification

Classification made for transcript

Verdict is Benign. Variant got -15 ACMG points.

BP4

Computational evidence support a benign effect (BayesDel_noAF=-0.53).

BP6

Variant 6-33195674-G-A is Benign according to our data. Variant chr6-33195674-G-A is described in ClinVar as [Benign]. Clinvar id is 1254260.Status of the report is criteria_provided_single_submitter, 1 stars.

BP7

Synonymous conserved (PhyloP=2.99 with no splicing effect.

BA1

GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.946 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
RXRB	NM_021976.5 linkuse as main transcript	c.1152C>T	p.Phe384=	synonymous_variant	7/10	ENST00000374680.4	NP_068811.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
RXRB	ENST00000374680.4 linkuse as main transcript	c.1152C>T	p.Phe384=	synonymous_variant	7/10	1	NM_021976.5	ENSP00000363812	P4	P28702-1
RXRB	ENST00000374685.8 linkuse as main transcript	c.1152C>T	p.Phe384=	synonymous_variant	7/10	1		ENSP00000363817	A1	P28702-3
RXRB	ENST00000483281.5 linkuse as main transcript	c.*664C>T		3_prime_UTR_variant, NMD_transcript_variant	6/9	5		ENSP00000431369

Frequencies

GnomAD3 genomes

AF:

0.771

AC:

117207

AN:

151966

Hom.:

45589

Cov.:

show subpopulations

Gnomad AFR

AF:

0.835

Gnomad AMI

AF:

0.605

Gnomad AMR

AF:

0.784

Gnomad ASJ

AF:

0.800

Gnomad EAS

AF:

0.968

Gnomad SAS

AF:

0.872

Gnomad FIN

AF:

0.708

Gnomad MID

AF:

0.816

Gnomad NFE

AF:

0.717

Gnomad OTH

AF:

0.791

GnomAD3 exomes

AF:

0.775

AC:

190210

AN:

245492

Hom.:

74523

AF XY:

0.776

AC XY:

103808

AN XY:

133834

show subpopulations

Gnomad AFR exome

AF:

0.840

Gnomad AMR exome

AF:

0.794

Gnomad ASJ exome

AF:

0.810

Gnomad EAS exome

AF:

0.974

Gnomad SAS exome

AF:

0.859

Gnomad FIN exome

AF:

0.699

Gnomad NFE exome

AF:

0.715

Gnomad OTH exome

AF:

0.774

GnomAD4 exome

AF:

0.737

AC:

1075707

AN:

1460260

Hom.:

399087

Cov.:

AF XY:

0.740

AC XY:

537907

AN XY:

726424

show subpopulations

Gnomad4 AFR exome

AF:

0.848

Gnomad4 AMR exome

AF:

0.797

Gnomad4 ASJ exome

AF:

0.810

Gnomad4 EAS exome

AF:

0.981

Gnomad4 SAS exome

AF:

0.857

Gnomad4 FIN exome

AF:

0.702

Gnomad4 NFE exome

AF:

0.711

Gnomad4 OTH exome

AF:

0.755

GnomAD4 genome

AF:

0.771

AC:

117302

AN:

152084

Hom.:

45628

Cov.:

AF XY:

0.772

AC XY:

57400

AN XY:

74322

show subpopulations

Gnomad4 AFR

AF:

0.835

Gnomad4 AMR

AF:

0.784

Gnomad4 ASJ

AF:

0.800

Gnomad4 EAS

AF:

0.968

Gnomad4 SAS

AF:

0.871

Gnomad4 FIN

AF:

0.708

Gnomad4 NFE

AF:

0.717

Gnomad4 OTH

AF:

0.794

Alfa

AF:

0.737

Hom.:

59707

Bravo

AF:

0.781

Asia WGS

AF:

0.879

AC:

3057

AN:

3478

EpiCase

AF:

0.732

EpiControl

AF:

0.739

ClinVar

Significance: Benign

Submissions summary: Benign:2

Revision: criteria provided, single submitter

LINK: link

Submissions by phenotype

RXRB-related disorder

Benign:1

Benign, no assertion criteria provided

clinical testing

PreventionGenetics, part of Exact Sciences

Oct 16, 2019

This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). -

not provided

Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

Sep 27, 2019

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.53

CADD

Benign

DANN

Benign

0.87

Splicing

Name

Calibrated prediction

Score

Prediction

SpliceAI score (max)

0.060

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