rs4657093

chr1-161723213-T-C

Variant summary

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

The NM_001002901.4(FCRLB):c.53-154T>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.181 in 152,026 control chromosomes in the GnomAD database, including 2,848 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 0.18 (2848 hom., cov: 31)
• Consequence: FCRLB NM_001002901.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.0720

Genes affected

FCRLB (HGNC:26431): (Fc receptor like B) FCRL2 belongs to the Fc receptor family. Fc receptors are involved in phagocytosis, antibody-dependent cell cytotoxicity, immediate hypersensitivity, and transcytosis of immunoglobulins via their ability to bind immunoglobulin (Ig) constant regions (Chikaev et al., 2005 [PubMed 15676285]).[supplied by OMIM, Mar 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.86).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.303 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	UniProt
FCRLB	NM_001002901.4	c.53-154T>C		intron_variant		ENST00000367948.7

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Appris	UniProt
FCRLB	ENST00000367948.7	c.53-154T>C		intron_variant		1	NM_001002901.4	P1

Frequencies

GnomAD3 genomes AF: 0.181 AC: 27465 AN: 151908 Hom.: 2833 Cov.: 31

Gnomad AFR AF: 0.224

Gnomad AMI AF: 0.0899

Gnomad AMR AF: 0.309

Gnomad ASJ AF: 0.212

Gnomad EAS AF: 0.150

Gnomad SAS AF: 0.120

Gnomad FIN AF: 0.155

Gnomad MID AF: 0.180

Gnomad NFE AF: 0.136

Gnomad OTH AF: 0.199

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

GnomAD4 genome AF: 0.181 AC: 27502 AN: 152026 Hom.: 2848 Cov.: 31 AF XY: 0.182 AC XY: 13548 AN XY: 74308

Gnomad4 AFR AF: 0.224

Gnomad4 AMR AF: 0.310

Gnomad4 ASJ AF: 0.212

Gnomad4 EAS AF: 0.149

Gnomad4 SAS AF: 0.120

Gnomad4 FIN AF: 0.155

Gnomad4 NFE AF: 0.136

Gnomad4 OTH AF: 0.197

Alfa AF: 0.159 Hom.: 2890

Bravo AF: 0.199

Asia WGS AF: 0.185 AC: 646 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.86
Cadd	Benign	0.41
Dann	Benign	0.70

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.040		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: rs4657093; hg19: chr1-161693003; COSMIC: COSV61060211; COSMIC: COSV61060211;