2-112542817-A-C

Variant summary

Our verdict is Benign. Variant got -14 ACMG points: 0P and 14B. BP4_Strong BP6_Moderate BA1

The NM_019014.6(POLR1B):c.177+146A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.565 in 1,005,258 control chromosomes in the GnomAD database, including 163,249 homozygotes. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency:
  • Genomes: 𝑓 0.54 (22078 hom., cov: 32)
  • Exomes 𝑓: 0.57 (141171 hom.)
• Consequence: POLR1B NM_019014.6 intron
• Clinical Significance: Benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.201

Genes affected

POLR1B (HGNC:20454): (RNA polymerase I subunit B) Eukaryotic RNA polymerase I (pol I) is responsible for the transcription of ribosomal RNA (rRNA) genes and production of rRNA, the primary component of ribosomes. Pol I is a multisubunit enzyme composed of 6 to 14 polypeptides, depending on the species. Most of the mass of the pol I complex derives from the 2 largest subunits, Rpa1 and Rpa2 in yeast. POLR1B is homologous to Rpa2 (Seither and Grummt, 1996 [PubMed 8921381]).[supplied by OMIM, Mar 2008]

ACMG classification

Verdict is Benign. Variant got -14 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.93).
• BP6: Variant 2-112542817-A-C is Benign according to our data. Variant chr2-112542817-A-C is described in ClinVar as [Benign]. Clinvar id is 1267427.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: GnomAd4 highest subpopulation (NFE) allele frequency at 95% confidence interval = 0.581 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
POLR1B	NM_019014.6	c.177+146A>C		intron_variant		ENST00000263331.10

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
POLR1B	ENST00000263331.10	c.177+146A>C		intron_variant		2	NM_019014.6	P1

Frequencies

GnomAD3 genomes AF: 0.535 AC: 81338 AN: 151948 Hom.: 22062 Cov.: 32

Gnomad AFR AF: 0.493

Gnomad AMI AF: 0.485

Gnomad AMR AF: 0.510

Gnomad ASJ AF: 0.627

Gnomad EAS AF: 0.362

Gnomad SAS AF: 0.498

Gnomad FIN AF: 0.477

Gnomad MID AF: 0.658

Gnomad NFE AF: 0.586

Gnomad OTH AF: 0.576

GnomAD4 exome AF: 0.570 AC: 486087 AN: 853192 Hom.: 141171 Cov.: 11 AF XY: 0.568 AC XY: 243333 AN XY: 428514

Gnomad4 AFR exome AF: 0.503

Gnomad4 AMR exome AF: 0.475

Gnomad4 ASJ exome AF: 0.627

Gnomad4 EAS exome AF: 0.341

Gnomad4 SAS exome AF: 0.506

Gnomad4 FIN exome AF: 0.477

Gnomad4 NFE exome AF: 0.596

Gnomad4 OTH exome AF: 0.560

GnomAD4 genome AF: 0.535 AC: 81387 AN: 152066 Hom.: 22078 Cov.: 32 AF XY: 0.528 AC XY: 39226 AN XY: 74306

Gnomad4 AFR AF: 0.494

Gnomad4 AMR AF: 0.510

Gnomad4 ASJ AF: 0.627

Gnomad4 EAS AF: 0.360

Gnomad4 SAS AF: 0.496

Gnomad4 FIN AF: 0.477

Gnomad4 NFE AF: 0.586

Gnomad4 OTH AF: 0.578

Alfa AF: 0.549 Hom.: 2869

Bravo AF: 0.536

Asia WGS AF: 0.451 AC: 1567 AN: 3478

ClinVar

Significance: Benign

Submissions summary: Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

not provided Benign:1

Benign, criteria provided, single submitter

clinical testing

GeneDx

May 14, 2021

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Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.93
Cadd	Benign	4.1
Dann	Benign	0.63

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.050		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: rs4849072; hg19: chr2-113300394;