NM_022763.4:c.-29+23202A>G

Variant names:

• chr3-172062973-A-G
• rs4894796
• NM_022763.4:c.-29+23202A>G

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_022763.4(FNDC3B):​c.-29+23202A>G variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.534 in 152,004 control chromosomes in the GnomAD database, including 22,027 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 0.53 (22027 hom., cov: 32)
• Consequence: FNDC3B NM_022763.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.04
• Publications: 10 publications found

Genes affected

FNDC3B (HGNC:24670): (fibronectin type III domain containing 3B) Enables RNA binding activity. Predicted to act upstream of or within several processes, including negative regulation of osteoblast differentiation; substrate adhesion-dependent cell spreading; and type II pneumocyte differentiation. Predicted to be located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.85).
• BA1: GnomAd4 highest subpopulation (AMR) allele frequency at 95% confidence interval = 0.581 is higher than 0.05.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_022763.4. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FNDC3B	NM_022763.4	MANE Select	c.-29+23202A>G		intron	N/A	NP_073600.3
	FNDC3B	NM_001135095.2		c.-29+22349A>G		intron	N/A	NP_001128567.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	FNDC3B	ENST00000415807.7	TSL:1 MANE Select	c.-29+23202A>G		intron	N/A	ENSP00000411242.2
	FNDC3B	ENST00000336824.8	TSL:1	c.-29+22349A>G		intron	N/A	ENSP00000338523.4
	FNDC3B	ENST00000416957.5	TSL:1	c.-29+16026A>G		intron	N/A	ENSP00000389094.1

Frequencies

GnomAD3 genomes AF: 0.534 AC: 81087 AN: 151886 Hom.: 22000 Cov.: 32

Gnomad AFR AF: 0.432

Gnomad AMI AF: 0.642

Gnomad AMR AF: 0.591

Gnomad ASJ AF: 0.501

Gnomad EAS AF: 0.539

Gnomad SAS AF: 0.470

Gnomad FIN AF: 0.600

Gnomad MID AF: 0.433

Gnomad NFE AF: 0.577

Gnomad OTH AF: 0.558

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

GnomAD4 genome AF: 0.534 AC: 81154 AN: 152004 Hom.: 22027 Cov.: 32 AF XY: 0.537 AC XY: 39873 AN XY: 74298

African (AFR) AF: 0.432 AC: 17915 AN: 41446

American (AMR) AF: 0.591 AC: 9028 AN: 15270

Ashkenazi Jewish (ASJ) AF: 0.501 AC: 1739 AN: 3472

East Asian (EAS) AF: 0.538 AC: 2781 AN: 5168

South Asian (SAS) AF: 0.471 AC: 2273 AN: 4828

European-Finnish (FIN) AF: 0.600 AC: 6341 AN: 10568

Middle Eastern (MID) AF: 0.438 AC: 128 AN: 292

European-Non Finnish (NFE) AF: 0.577 AC: 39175 AN: 67938

Other (OTH) AF: 0.563 AC: 1190 AN: 2112

Alfa AF: 0.558 Hom.: 57939

Bravo AF: 0.530

Asia WGS AF: 0.549 AC: 1908 AN: 3474

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.85
CADD	Benign	0.71
DANN	Benign	0.83
PhyloP100		-1.0
RBP_binding_hub_radar		0.0
RBP_regulation_power_radar		1.1
Mutation Taster		=100/0	polymorphism (auto)

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

Other links and lift over

dbSNP: rs4894796; hg19: chr3-171780763;