chr19-41862174-G-T

Position:

• chr19-41862174-G-T

Variant summary

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

The NM_001022.4(RPS19):​c.172+962G>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.458 in 152,042 control chromosomes in the GnomAD database, including 16,789 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 0.46 (16789 hom., cov: 32)
• Consequence: RPS19 NM_001022.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.391

Genes affected

RPS19 (HGNC:10402): (ribosomal protein S19) 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 S19E family of ribosomal proteins. It is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia (DBA), a constitutional erythroblastopenia characterized by absent or decreased erythroid precursors, in a subset of patients. This suggests a possible extra-ribosomal function for this gene in erythropoietic differentiation and proliferation, in addition to its ribosomal function. Higher expression levels of this gene in some primary colon carcinomas compared to matched normal colon tissues has been observed. 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]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (Cadd=2.173).
• BA1: GnomAd4 highest subpopulation (SAS) allele frequency at 95% confidence interval = 0.556 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
RPS19	NM_001022.4	c.172+962G>T		intron_variant		ENST00000598742.6	NP_001013.1
RPS19	NM_001321483.2	c.172+962G>T		intron_variant			NP_001308412.1
RPS19	NM_001321484.2	c.172+962G>T		intron_variant			NP_001308413.1
RPS19	NM_001321485.2	c.185+949G>T		intron_variant			NP_001308414.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
RPS19	ENST00000598742.6	c.172+962G>T		intron_variant		1	NM_001022.4	ENSP00000470972	P1

Frequencies

GnomAD3 genomes AF: 0.458 AC: 69534 AN: 151924 Hom.: 16772 Cov.: 32

Gnomad AFR AF: 0.295

Gnomad AMI AF: 0.565

Gnomad AMR AF: 0.507

Gnomad ASJ AF: 0.654

Gnomad EAS AF: 0.461

Gnomad SAS AF: 0.575

Gnomad FIN AF: 0.516

Gnomad MID AF: 0.687

Gnomad NFE AF: 0.514

Gnomad OTH AF: 0.509

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

GnomAD4 genome AF: 0.458 AC: 69591 AN: 152042 Hom.: 16789 Cov.: 32 AF XY: 0.463 AC XY: 34378 AN XY: 74314

Gnomad4 AFR AF: 0.296

Gnomad4 AMR AF: 0.507

Gnomad4 ASJ AF: 0.654

Gnomad4 EAS AF: 0.461

Gnomad4 SAS AF: 0.574

Gnomad4 FIN AF: 0.516

Gnomad4 NFE AF: 0.514

Gnomad4 OTH AF: 0.504

Alfa AF: 0.390 Hom.: 1550

Bravo AF: 0.446

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
CADD	Benign	2.2

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs3786538; hg19: -;