Genetic Variant RPS25:n.304C>A (chr11-119018363-G-T) – ACMG Classification: Benign (-20 pts)

Variant summary

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

The ENST00000527791.5(RPS25):n.-79C>A variant causes a non coding transcript exon change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.0922 in 1,602,904 control chromosomes in the GnomAD database, including 8,241 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★★).

Frequency

Genomes: 𝑓 0.073 ( 575 hom., cov: 33)

Exomes 𝑓: 0.094 ( 7666 hom. )

Consequence

RPS25
ENST00000527791.5 non_coding_transcript_exon

Scores

Clinical Significance

Benign criteria provided, multiple submitters, no conflicts B:2

Conservation

PhyloP100: -0.289

Variant links:

Genes affected

RPS25 (HGNC:10413): (ribosomal protein S25) Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S25E family of ribosomal proteins. It is located in the cytoplasm. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]

RPS25 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=-0.8).

BP6

Variant 11-119018363-G-T is Benign according to our data. Variant chr11-119018363-G-T is described in ClinVar as [Benign]. Clinvar id is 1264702.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.

BA1

GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.223 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
RPS25	NM_001028.3 link	c.-79C>A		upstream_gene_variant		ENST00000527673.2	NP_001019.1	P62851

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
RPS25	ENST00000527673.2 link	c.-79C>A		upstream_gene_variant		1	NM_001028.3	ENSP00000435096.1		P62851

Frequencies

GnomAD3 genomes

AF:

0.0731

AC:

11114

AN:

152138

Hom.:

573

Cov.:

show subpopulations

Gnomad AFR

AF:

0.0310

Gnomad AMI

AF:

0.0976

Gnomad AMR

AF:

0.0543

Gnomad ASJ

AF:

0.0325

Gnomad EAS

AF:

0.0606

Gnomad SAS

AF:

0.234

Gnomad FIN

AF:

0.145

Gnomad MID

AF:

0.0886

Gnomad NFE

AF:

0.0835

Gnomad OTH

AF:

0.0565

GnomAD4 exome

AF:

0.0942

AC:

136605

AN:

1450648

Hom.:

7666

Cov.:

AF XY:

0.0979

AC XY:

70675

AN XY:

721628

show subpopulations

Gnomad4 AFR exome

AF:

0.0280

Gnomad4 AMR exome

AF:

0.0596

Gnomad4 ASJ exome

AF:

0.0400

Gnomad4 EAS exome

AF:

0.0761

Gnomad4 SAS exome

AF:

0.221

Gnomad4 FIN exome

AF:

0.137

Gnomad4 NFE exome

AF:

0.0880

Gnomad4 OTH exome

AF:

0.0886

GnomAD4 genome

AF:

0.0731

AC:

11124

AN:

152256

Hom.:

575

Cov.:

AF XY:

0.0775

AC XY:

5766

AN XY:

74442

show subpopulations

Gnomad4 AFR

AF:

0.0310

Gnomad4 AMR

AF:

0.0542

Gnomad4 ASJ

AF:

0.0325

Gnomad4 EAS

AF:

0.0607

Gnomad4 SAS

AF:

0.234

Gnomad4 FIN

AF:

0.145

Gnomad4 NFE

AF:

0.0834

Gnomad4 OTH

AF:

0.0607

Alfa

AF:

0.0340

Hom.:

Bravo

AF:

0.0604

Asia WGS

AF:

0.155

AC:

541

AN:

3478

ClinVar

Significance: Benign

Submissions summary: Benign:2

Revision: criteria provided, multiple submitters, no conflicts

LINK: link

Submissions by phenotype

not provided

Benign:2

Breakthrough Genomics, Breakthrough Genomics

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: not provided

- -

May 15, 2021

GeneDx

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

- -

Computational scores

Source: dbNSFP v4.3

Name

Calibrated prediction

Score

Prediction

BayesDel_noAF

Benign

-0.80

CADD

Benign

0.27

DANN

Benign

0.77

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

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